Novel piperidine derivatives

ABSTRACT

The present invention provides a compound of a formula (I): 
     
       
         
         
             
             
         
       
     
     wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a chemokine (such as CCR3) mediated disease state.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.11/996,133, which is a national phase application under 35 U.S.C. §371of PCT International Application No. PCT/SE2006/000893, filed Jul. 19,2006, which claims the benefit of Swedish Application Serial No.0501719-9, filed Jul. 21, 2005, and Swedish Application Serial No.0600838-7, filed Apr. 13, 2006. Each of these prior applications isincorporated herein by reference in their entirety.

The present invention concerns piperidine derivatives havingpharmaceutical activity, to processes for preparing such derivatives, topharmaceutical compositions comprising such derivatives and to the useof such derivatives as active therapeutic agents.

Pharmaceutically active piperidine derivatives are disclosed in WO2004/087659.(2S)-2-[4-[[4-(3,4-Dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid and its dihydrochloride salt are disclosed in WO 2004/087659 (seeexamples 40 and 73). Compounds of present invention have higher potencyat CCR3 than comparable compounds in WO 2004/087659 [which translates toa lower dose meaning less serious side-effects, for example at the IKrchannel (for example using the assay described in WO 2005/037052, or theelectrophysiology method described in the paper: ‘Optimisation andvalidation of a medium-throughput electrophysiology-based hERG assayusing IonWorks™ HT’ by M. H. Bridgland-Taylor, C. E. Pollard et al inJournal of Pharmacological and Toxicological Methods (2006; available onthe internet Elsevier publications www.sciencedirect.com, and inpress))]. The higher potency of the compounds of the invention alsotranslates to increased selectivity over the histamine type 1 (H1)receptor.

Histamine is a basic amine, 2-(4-imidazolyl)-ethylamine, and is formedfrom histidine by histidine decarboxylase. It is found in most tissuesof the body, but is present in high concentrations in the lung, skin andin the gastrointestinal tract. At the cellular level inflammatory cellssuch as mast cells and basophils store large amounts of histamine. It isrecognised that the degranulation of mast cells and basophils and thesubsequent release of histamine is a fundamental mechanism responsiblefor the clinical manifestation of an allergic process. Histamineproduces its actions by an effect on specific histamine G-proteincoupled receptors, which are of three main types, H1, H2 and H3.Histamine H1 antagonists comprise the largest class of medications usedin the treatment of patients with allergic disorders, for examplerhinitis or urticaria. H1 antagonists are useful in controlling theallergic response by for example blocking the action of histamine onpost-capillary venule smooth muscle, resulting in decreased vascularpermeability, exudation and oedema. The antagonists also produceblockade of the actions of histamine on the H1 receptors on c-typenociceptive nerve fibres, resulting in decreased itching and sneezing.

Chemokines are chemotactic cytokines that are released by a wide varietyof cells to attract macrophages, T cells, eosinophils, basophils andneutrophils to sites of inflammation and also play a role in thematuration of cells of the immune system. Chemokines play an importantrole in immune and inflammatory responses in various diseases anddisorders, including asthma and allergic diseases, as well as autoimmunepathologies such as rheumatoid arthritis and atherosclerosis. Thesesmall secreted molecules are a growing superfamily of 8-14 kDa proteinscharacterised by a conserved four cysteine motif. The chemokinesuperfamily can be divided into two main groups exhibitingcharacteristic structural motifs, the Cys-X-Cys (C-X-C, or α) andCys-Cys (C-C, or β) families. These are distinguished on the basis of asingle amino acid insertion between the NH-proximal pair of cysteineresidues and sequence similarity.

The C-X-C chemokines include several potent chemoattractants andactivators of neutrophils such as interleukin-8 (IL-8) andneutrophil-activating peptide 2 (NAP-2).

The C-C chemokines include potent chemoattractants of monocytes andlymphocytes but not neutrophils such as human monocyte chemotacticproteins 1-3 (MCP-1, MCP-2 and MCP-3), RANTES (Regulated on Activation,Normal T Expressed and Secreted), eotaxin, eotaxin-2, eotaxin-3 and themacrophage inflammatory proteins 1α and 1β (MIP-1α and MIP-1β.

Studies have demonstrated that the actions of the chemokines aremediated by subfamilies of G protein-coupled receptors, among which arethe receptors designated CCR1, CCR2, CCR2A, CCR2B, CCR3, CCR4, CCR5,CCR6, CCR7, CCR8, CCR9, CCR10, CXCR1, CXCR2, CXCR3 and CXCR4. Thesereceptors represent good targets for drug development since agents whichmodulate these receptors would be useful in the treatment of disordersand diseases such as those mentioned above.

Viral infections are known to cause lung inflammation. It has been shownexperimentally that the common cold increases mucosal output of eotaxinin the airways. Instillation of eotaxin into the nose can mimic some ofthe signs and symptoms of a common cold. (See, Greiff L et at Allergy(1999) 54(11) 1204-8 [Experimental common cold increase mucosal outputof eotaxin in atopic individuals] and Kawaguchi M et at Int. Arch.Allergy Immunol. (2000) 122 S1 44 [Expression of eotaxin by normalairway epithelial cells after virus A infection].)

The present invention provides a compound of formula (I):

to wherein:R¹ is phenyl optionally substituted by halogen, cyano, C₁₋₄ alkyl orC₁₋₄ alkoxy;R² is methyl or ethyl;R is hydrogen, or CO₂R is (CO₂ ⁻)_(p)R^(p+) wherein R^(p+) is aunivalent cation (for example an alkali metal cation) or twocarboxylates may coordinate a divalent cation (for example an alkalineearth metal cation);p is 1 or 2;R³ is phenyl optionally substituted with halogen, cyano, C₁₋₄ alkyl,C₁₋₄ alkoxy, CF₃ or OCF₃;when R¹ is 2-methyl-3,4-dichlorophenyl and R³ is 4-fluorophenyl,4-cyanophenyl or 2-methoxyphenyl, then R² can also be hydrogen;or an N-oxide thereof; or a pharmaceutically acceptable salt thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the XRPD of Form I (as described in Example 28).

FIG. 2 shows the XRPD of Form II (as described in Example 29).

FIG. 3 shows the XRPD of Form A (as described in Example 32).

FIG. 4 shows the XRPD for(2S)-2-(4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid ethanol solvate Form B (as described in Example 34).

Compounds of formula (I) wherein R² is methyl are surprisingly moresoluble (sometimes up to 10 times more soluble) in certain solvents (forexample phosphate buffer at pH 7.4) than compounds of formula (I)wherein R² is hydrogen. The increased solubility is advantageous for aoral pharmaceutical as the active ingredient will be more readilyavailable for absorption from the gastrointestinal tract.

Certain compounds of the present invention can exist in differentisomeric forms (such as enantiomers, diastereomers, geometric isomers ortautomers). The present invention covers all such isomers and mixturesthereof in all proportions.

The compounds of the invention can be zwitterionic and all suchzwitterions are within the invention.

Suitable pharmaceutically acceptable salts include acid addition saltssuch as a hydrochloride, dihydrochloride, hydrobromide, phosphate,sulfate, acetate, fumarate, maleate, malonate, succinate, tartrate,citrate, oxalate, methanesulfonate, benzenesulfonate orp-toluenesulfonic acid. (CO₂ ⁻)_(p)R^(p+) are salts of the invention.

An alkali metal cation is, for example sodium or potassium, and analkaline earth metal cation is, for example, magnesium or calcium.

The univalent cation R^(p+), wherein p is 1, can also be, for example, aprotonated tertiary amine such as (CH₂CH₂OH)₃NH′.

The compounds of the invention may exist as solvates (such as hydrates)and the present invention covers all such solvates. Examples ofalternative solvates include compounds of the invention having ethanolor ethyl acetate included in the solid phase. Solvates can exist as, forexample, a compound of the invention having solvate molecules within thecrystal lattice, or, where solvent is within one or more channels withinthe crystal lattice (such as a channel hydrate), or a mixture of thesetwo.

Halogen includes fluorine, chlorine, bromine and iodine. Halogen is, forexample, fluorine or chlorine.

Alkyl is straight or branched chain and is, for example, methyl, ethyl,n-propyl, iso-propyl or tert-butyl.

In one particular aspect the present invention provides a compound offormula (I) wherein: R¹ is phenyl optionally substituted by halogen,cyano, C₁₋₄ alkyl or C₁₋₄ alkoxy; R² is methyl; R is hydrogen, or CO₂Ris (CO₂ ⁻)_(p)R^(p+) wherein R^(p+) is a univalent cation (for examplean alkali metal cation) or two carboxylates may coordinate a divalentcation (for example an alkaline earth metal cation); p is 1 or 2; R³ isphenyl optionally substituted with halogen, cyano, C₁₋₄ alkyl, C₁₋₄alkoxy, CF₃ or OCF₃; when R¹ is 2-methyl-3,4-dichlorophenyl and R³ is4-fluorophenyl, 4-cyanophenyl or 2-methoxyphenyl, then R² can also behydrogen; or an N-oxide thereof; or a pharmaceutically acceptable saltthereof.

In a further aspect the present invention provides a compound of formula(I) wherein: R¹ is phenyl optionally substituted by halogen, cyano, C₁₋₄alkyl or C₁₋₄ alkoxy; R² is methyl; R is hydrogen, or CO₂R is (CO₂⁻)_(p)R^(p+) wherein R^(p+) is a univalent cation (for example an alkalimetal cation) or two carboxylates may coordinate a divalent cation (forexample an alkaline earth metal cation); p is 1 or 2; R³ is phenyloptionally substituted with halogen, cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy, CF₃or OCF₃; when R¹ is 2-methyl-3,4-dichlorophenyl and R³ is4-fluorophenyl, 4-cyanophenyl or 2-methoxyphenyl, then R² can also behydrogen; or a pharmaceutically acceptable salt thereof.

In another aspect the present invention provides a compound of formula(I) wherein, R¹ is phenyl optionally substituted by halogen, cyano, C₁₋₄alkyl or C₁₋₄ alkoxy; R² is methyl; R is hydrogen, or CO₂R is (CO₂⁻)_(p)R^(p+) wherein R^(p+) is a univalent cation (for example an alkalimetal cation) or two carboxylates may coordinate a divalent cation (forexample an alkaline earth metal cation); p is 1 or 2; R³ is phenyloptionally substituted with halogen, cyano, C₁₋₄ alkyl, C₁₋₄ alkoxy, CF₃or OCF₃; or a pharmaceutically acceptable salt thereof.

In a further aspect the present invention provides a compound wherein R¹is phenyl optionally substituted (for example with two or three of thesame or different) with fluorine, chlorine, cyano, C₁₋₄ alkyl (forexample methyl) or C₁₋₄ alkoxy (for example methoxy).

In another aspect the present invention provides a compound wherein R¹is phenyl optionally substituted (for example with two or three of thesame or different) with fluorine, chlorine, cyano or C₁₋₄ alkyl (forexample methyl).

In yet another aspect the present invention provides a compound whereinR¹ is phenyl substituted by two or three substituents independentlyselected from: fluorine, chlorine, cyano and methyl.

In a further aspect the present invention provides a compound wherein R¹is phenyl substituted by two or three substituents independentlyselected from: chlorine and methyl.

For example R¹ is 3,4-dichlorophenyl, 4-chloro-2-methylphenyl,2,4-dichloro-3-methylphenyl or 3,4-dichloro-2-methylphenyl. R¹ can alsobe 4-fluoro-2-methylphenyl or 4-chloro-3-methylphenyl. For example R¹ is3,4-dichloro-2-methylphenyl. For example R¹ is 4-chloro-2-methylphenyl.

In a still further aspect the present invention provides a compound offormula (I) wherein R is hydrogen.

In another aspect the present invention provides a compound of formula(I) wherein CO₂R is CO₂ ⁻R⁺, wherein R⁺ is sodium or potassium.

In yet another aspect R² is methyl.

In a still further aspect the present invention provides a compound offormula (I) wherein R² is hydrogen and R³ is 4-fluorophenyl,4-cyanophenyl or 2-methoxyphenyl (for example R³ is 4-fluorophenyl).

The invention further provides(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid or a pharmaceutically acceptable salt thereof (for example asodium, potassium or (CH₂CH₂OH)₃NH⁺ salt, or an acid addition salt, suchas a hydrochloride, dihydrochloride, hydrobromide, phosphate, sulfate,acetate, fumarate, maleate, malonate, succinate, tartrate, citrate,oxalate, methanesulfonate, benzenesulfonate or p-toluenesulfonic acid).

In a still further aspect the present invention provides(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid.

In another aspect the present invention provides a polymorph of(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid hydrate (Form A) {water of varying stoichiometry, for example1.5-2.5 equivalents} having an X-ray powder diffraction patterncontaining specific peaks at: 5.3 (±0.1°), 10.6 (±0.1°), 12.3 (±0.1°),12.9 (±0.1°), 13.9 (±0.1°), 15.5 (±0.1°), 15.9 (±0.1°), 16.9 (±0.1°),19.6 (±0.1°), 20.0 (±0.1°), 20.4 (±0.1°), 21.1 (±0.1°), 21.5 (±0.1°),24.0 (±0.1°), 24.8 (±0.1°), 25.1 (±0.1°), 25.8 (±0.1°), 29.4 (±0.1°) and29.6 (±0.1°) 2θ.

In yet another aspect the present invention provides a polymorph of(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid ethanol solvate (Form B) having an X-ray powder diffraction patterncontaining specific peaks at: 7.7 (±0.1°), 13.3 (±0.1°), 15.2 (±0.1°),15.4 (±0.1°), 17.4) (±0.1°), 18.4 (±0.1°), 19.7 (±0.1°), 20.6 (±0.1°),21.7 (±0.1°) and 22.7 (±0.1°) 2θ.

In another aspect the present invention provides a compound wherein R³is phenyl optionally substituted with halogen (such as fluoro), cyano orC₁₋₄ alkoxy (such as methoxy).

In yet another aspect the present invention provides a compound offormula (I) wherein R² is methyl and R³ is fluorophenyl (for example4-fluorophenyl).

In another aspect the present invention provides(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid or a pharmaceutically acceptable salt thereof (for example asodium, potassium or (CH₂CH₂OH)₃NH⁺ salt, or an acid addition salt, suchas a hydrochloride, dihydrochloride, hydrobromide, phosphate, sulfate,acetate, fumarate, maleate, malonate, succinate, tartrate, citrate,oxalate, methanesulfonate, benzenesulfonate or p-toluenesulfonic acid).

In yet another aspect the present invention provides(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid.

In a further aspect the present invention provides a polymorph of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid (Form I) having an X-ray powder diffraction pattern containingspecific peaks at: 2.2 (±0.1°), 2.7 (±0.1°), 7.1 (±0.1°), 10.7 (±0.1°),13.3 (±0.1°) and 18.8 (±0.1°) 2θ.

In a still further aspect the present invention provides a polymorph of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid (Form II) having an X-ray powder diffraction pattern containingspecific peaks at: 2.2 (±0.1°), 2.67 (±0.1°), 7.2 (±0.1°), 13.2 (±0.1°),17.0 (±0.1°), 17.4 (±0.1°), 19.1 (±0.1°), 19.4 (±0.1°), 21.1 (±0.1°),24.4 (±0.1°) and 25.2 (±0.1°) 2θ.

In a further aspect the present invention provides a pharmaceuticallyacceptable salt of a compound of formula (I), having the (2S) absoluteconfiguration, wherein R¹ is 2-methyl-3,4-dichlorophenyl, R² is hydrogenand R³ is phenyl, provided it is not the dihydrochloride salt; such as amethanesulfonate or benzenesulfonate salt.

In another aspect the present invention provides a salt of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid, but not the dihydrochloride salt, [for example an alkali metalsalt (such as a sodium or potassium salt) or an acid addition salt (suchas one of those listed above, for example a methanesulfonic acid orbenzenesulfonic acid salt)]. In yet another aspect the present inventionprovides a sodium or potassium (for example a sodium salt) of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid.

In a further aspect the present invention provides one of the followingindividualised compounds of the invention:

-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-342-methoxyphenyl)-propanoic    acid;-   (2S)-3(4-cyanophenyl)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-propanoic    acid;-   (2S)-2-[4-[[4-(3,4-dichloro-2-ethyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoic    acid;-   (2S)-2-[4-[[4-(3,4-dichloro-2-ethyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid;

(2S)-2-(4-{[4-(3-chloro-4-cyano-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-phenylpropanoicacid;

(2S)-2-(4-{[4-(3-chloro-4-cyano-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)propanoicacid;

-   (2S)-2-[4-[[4-(2,4-dichloro-3-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid;-   (2S)-2-[4-[[4-(4-chloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid;-   (2S)-2-[4-[[4-(2,4-dichloro-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid;-   (S)-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoic    acid;-   (S)-2-[4-[[4-(4-chloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-2-methyl-propanoic    acid;-   (S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-2-methyl-propanoic    acid;-   Isomer 1 of    2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoic    acid;-   Isomer 2 of    2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoic    acid;-   2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-2-methyl-3-phenylpropanoic    acid;-   Isomer 1 of    2-[4-[[4-(3,4-dichlorophenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoic    acid;-   Isomer 2 of    2-[4-[[4-(3,4-dichlorophenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoic    acid;-   (±)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoic    acid;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoic    acid sodium salt;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid sodium salt;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid potassium salt;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoic    acid methanesulfonic acid salt;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoic    acid benzenesulfonic acid salt;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid benzenesulfonic acid salt;-   (2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoic    acid hydrochloride;-   2-Benzyl-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)butanoic    acid;-   (S)-2-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-phenyl-propionic    acid;-   (S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionic    acid (Form I);-   (S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionic    acid (form II);-   (2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)propanoic    acid; or,-   s    (2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-phenylpropanoic    acid;    or a pharmaceutically acceptable salt thereof.

The compounds of the present invention can be prepared as describedbelow or by methods analogous to those described in WO 2004/087659 or WO2004/029041.

A compound of formula (I) can be prepared by reacting a compound offormula (II):

with a compound of formula (III):

wherein R is alkyl (for example C₁₋₆ alkyl) in the presence ofNaBH(OAc)₃ or NaBH₃(CN) in a suitable solvent (for example an aliphaticalcohol such as methanol or ethanol) at a suitable temperature (such asin the range 0° C. to 30° C.), and subsequent ester hydrolysis by usingor adapting the methods given in the Examples below.

A compound of formula (II) can be prepared by reacting a compound offormula (IV):

with lead tetra-acetate in dichloromethane or sodium periodate in water.

Alternatively a compound of formula (I) wherein R² represents H may beprepared by reaction of a compound of formula (V) with a compound offormula (VI)

wherein R is alkyl (for example C₁₋₆ alkyl) and L is a suitable leavinggroup (for example a sulfonate ester, typically triflate orpara-nitrobenzenesulfonate), in a suitable solvent, for exampledichloromethane or acetonitrile, at a temperature in the range 0-30° C.in the presence of a base, for example a tertiary amine, such astriethylamine, or an inorganic base, such as potassium carbonate; andsubsequent ester hydrolysis by using or adapting the methods given inthe Examples below.

The preparations of various phenoxy piperidines and other intermediatesare described in the literature and in WO 01/77101, WO 2004/087659 or WO2004/029041.

A compound of the present invention wherein R is hydrogen can beprepared by hydrolysis of the corresponding ester (prepared by a methodknown in the art) under standard hydrolysis conditions (for exampleusing lithium hydroxide, sodium hydroxide, potassium hydroxide or bariumhydroxide).

In the above processes it may be desirable or necessary to protect anacid group or a hydroxy or other potentially reactive group. Suitableprotecting groups and details of processes for adding and removing suchgroups may be found in “Protective Groups in Organic Synthesis”, 3rdEdition (1999) by Greene and Wuts.

In another aspect the present invention provides processes for thepreparation of compounds of formula (I).

In a further aspect the invention provides the intermediates:

Salts of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid can be prepared by using or adapting the methods of the Examples orby using or adapting methods known in the art.

The compounds of the invention and their pharmaceutically acceptablesalts have activity as pharmaceuticals, in particular as modulators ofchemokine receptor (for example CCR3) activity, and may be used in thetreatment of autoimmune, inflammatory, proliferative orhyperproliferative diseases, or immunologically-mediated diseases(including rejection of transplanted organs or tissues and AcquiredImmunodeficiency Syndrome (AIDS)).

Examples of these conditions are:

1. respiratory tract: obstructive diseases of the airways including:asthma, including bronchial, allergic, intrinsic, extrinsic,exercise-induced, drug-induced (including aspirin and NSAID-induced) anddust-induced asthma, both intermittent and persistent and of allseverities, and other causes of airway hyper-responsiveness; chronicobstructive pulmonary disease (COPD); bronchitis, including infectiousand eosinophilic bronchitis; emphysema; bronchiectasis; cystic fibrosis;sarcoidosis; farmer's lung and related diseases; hypersensitivitypneumonitis; lung fibrosis, including cryptogenic fibrosing alveolitis,idiopathic interstitial pneumonias, fibrosis complicatinganti-neoplastic therapy and chronic infection, including tuberculosisand aspergillosis and other fungal infections; complications of lungtransplantation; vasculitic and thrombotic disorders of the lungvasculature, and pulmonary hypertension; antitussive activity includingtreatment of chronic cough associated with inflammatory and secretoryconditions of the airways, and iatrogenic cough; acute and chronicrhinitis including rhinitis medicamentosa, and vasomotor rhinitis;perennial and seasonal allergic rhinitis including rhinitis nervosa (hayfever); nasal polyposis; acute viral infection including the commoncold, and infection due to respiratory syncytial virus (RSV), influenza,coronavirus (including SARS) or adenovirus; or eosinophilic esophagitis;2. bone and joints: arthritides associated with or includingosteoarthritis/osteoarthrosis, both primary and secondary to, forexample, congenital hip dysplasia; cervical and lumbar spondylitis, andlow back and neck pain; osteoporosis; rheumatoid arthritis and Still'sdisease; seronegative spondyloarthropathies including ankylosingspondylitis, psoriatic arthritis, reactive arthritis andundifferentiated spondarthropathy; septic arthritis and otherinfection-related arthopathies and bone disorders such as tuberculosis,including Potts' disease and Poncet's syndrome; acute and chroniccrystal-induced synovitis including urate gout, calcium pyrophosphatedeposition disease, and calcium apatite related tendon, bursal andsynovial inflammation; Behcet's disease; primary and secondary Sjogren'ssyndrome; systemic sclerosis and limited scleroderma; systemic lupuserythematosus, mixed connective tissue disease, and undifferentiatedconnective tissue disease; inflammatory myopathies includingdermatomyositits and polymyositis; polymalgia rheumatica; juvenilearthritis including idiopathic inflammatory arthritides of whateverjoint distribution and associated syndromes, and rheumatic fever and itssystemic complications; vasculitides including giant cell arteritis,Takayasu's arteritis, Churg-Strauss syndrome, polyarteritis nodosa,microscopic polyarteritis, and vasculitides associated with viralinfection, hypersensitivity reactions, cryoglobulins, and paraproteins;low back pain; Familial Mediterranean fever, Muckle-Wells syndrome, andFamilial Hibernian Fever, Kikuchi disease; drug-induced arthalgias,tendonititides, and myopathies;3. pain and connective tissue remodelling of musculoskeletal disordersdue to injury [for example sports injury] or disease: arthritides (forexample rheumatoid arthritis, osteoarthritis, gout or crystalarthropathy), other joint disease (such as intervertebral discdegeneration or temporomandibular joint degeneration), bone remodellingdisease (such as osteoporosis, Paget's disease or osteonecrosis),polychondritits, scleroderma, mixed connective tissue disorder,spondyloarthropathies or periodontal disease (such as periodontitis);4. skin: psoriasis, atopic dermatitis, contact dermatitis or othereczematous dermatoses, and delayed-type hypersensitivity reactions;phyto- and photodermatitis; seborrhoeic dermatitis, dermatitisherpetiformis, lichen planus, lichen sclerosus et atrophica, pyodermagangrenosum, skin sarcoid, discoid lupus erythematosus, pemphigus,pemphigoid, epidermolysis bullosa, urticaria, angioedema, vasculitides,toxic erythemas, cutaneous eosinophilias, alopecia greata, male-patternbaldness, Sweet's syndrome, Weber-Christian syndrome, erythemamultiforme; cellulitis, both infective and non-infective; panniculitis;cutaneous lymphomas, non-melanoma skin cancer and other dysplasticlesions; drug-induced disorders including fixed drug eruptions;5. eyes: blepharitis; conjunctivitis, including perennial and vernalallergic conjunctivitis; iritis; anterior and posterior uveitis;choroiditis; autoimmune; degenerative or inflammatory disordersaffecting the retina; ophthalmitis including sympathetic ophthalmitis;sarcoidosis; infections including viral, fungal, and bacterial;6. gastrointestinal tract: glossitis, gingivitis, periodontitis;oesophagitis, including reflux; eosinophilic gastro-enteritis,mastocytosis, Crohn's disease, colitis (including ulcerative colitis,microscopic colitis and indeterminant colitis), proctitis, pruritis ani;coeliac disease, irritable bowel syndrome, irritable bowel disorder,non-inflammatory diarrhea, and food-related allergies which may haveeffects remote from the gut (for example migraine, rhinitis or eczema);7. abdominal: hepatitis, including autoimmune, alcoholic and viral;fibrosis and cirrhosis of the liver; cholecystitis; pancreatitis, bothacute and chronic;8. genitourinary: nephritis including interstitial andglomerulonephritis; nephrotic syndrome; cystitis including acute andchronic (interstitial) cystitis and Hunner's ulcer; acute and chronicurethritis, prostatitis, epididymitis, oophoritis and salpingitis;vulvo-vaginitis; Peyronie's disease; erectile dysfunction (both male andfemale);9. allograft rejection: acute and chronic following, for example,transplantation of kidney, heart, liver, lung, bone marrow, skin orcornea or following blood transfusion; or chronic graft versus hostdisease;10. CNS: Alzheimer's disease and other dementing disorders including CJDand nvCJD; amyloidosis; multiple sclerosis and other demyelinatingsyndromes; cerebral atherosclerosis and vasculitis; temporal arteritis;myasthenia gravis; acute and chronic pain (acute, intermittent orpersistent, whether of central or peripheral origin) including visceralpain, headache, migraine, trigeminal neuralgia, atypical facial pain,joint and bone pain, pain arising from cancer and tumour invasion,neuropathic pain syndromes including diabetic, post-herpetic, andHIV-associated neuropathies; neurosarcoidosis; central and peripheralnervous system complications of malignant, infectious or autoimmuneprocesses;11. other auto-immune and allergic disorders including Hashimoto'sthyroiditis, Graves' disease, Addison's disease, diabetes mellitus,idiopathic thrombocytopaenic purpura, eosinophilic fasciitis, hyper-IgEsyndrome, antiphospholipid syndrome;12. other disorders with an inflammatory or immunological component;including acquired immune deficiency syndrome (AIDS), leprosy, Sezarysyndrome, and paraneoplastic syndromes;13. cardiovascular: atherosclerosis, affecting the coronary andperipheral circulation; pericarditis; myocarditis, inflammatory andauto-immune cardiomyopathies including myocardial sarcoid; ischaemicreperfusion injuries; endocarditis, valvulitis, and aortitis includinginfective (for example syphilitic); vasculitides; disorders of theproximal and peripheral veins including phlebitis and thrombosis,including deep vein thrombosis and complications of varicose veins; or,14. oncology: treatment of common cancers including prostate, breast,lung, ovarian, pancreatic, bowel and colon, stomach, skin and braintumours and malignancies affecting the bone marrow (including theleukaemias) and lymphoproliferative systems, such as Hodgkin's andnon-Hodgkin's lymphoma; including the prevention and treatment ofmetastatic disease and tumour recurrences, and paraneoplastic syndromes.

According to a further feature of the present invention there isprovided a method for treating a chemokine mediated disease state (forexample a CCR3 mediated disease state) in a mammal, such as man,suffering from, or at risk of, said disease state, which comprisesadministering to a mammal in need of such treatment a therapeuticallyeffective amount of a compound of the invention or a pharmaceuticallyacceptable salt thereof.

According to yet another feature of the present invention there isprovided a method for treating a sign and/or symptom of what is commonlyreferred to as a cold in a mammal, such as man, suffering from, or atrisk of, said disease state, which comprises administering to a mammalin need of such treatment a therapeutically effective amount of acompound of the invention or a pharmaceutically acceptable salt thereof.

The invention also provides a compound of the invention, or apharmaceutically acceptable salt thereof, for use in therapy.

In another aspect the invention provides the use of a compound of theinvention, or a pharmaceutically acceptable salt thereof, in themanufacture of a medicament for use in therapy (for example modulatingchemokine receptor activity (for example CCR3 receptor activity) ortreating a sign and/or symptom of what is commonly referred to as acold).

The invention further provides the use of a compound of the invention,or a pharmaceutically acceptable salt thereof, in the manufacture of amedicament for use in the treatment of:

1. respiratory tract: obstructive diseases of the airways including:asthma, including bronchial, allergic, intrinsic, extrinsic,exercise-induced, drug-induced (including aspirin and NSAID-induced) anddust-induced asthma, both intermittent and persistent and of allseverities, and other causes of airway hyper-responsiveness; chronicobstructive pulmonary disease (COPD); bronchitis, including infectiousand eosinophilic bronchitis; emphysema; bronchiectasis; cystic fibrosis;sarcoidosis; farmer's lung and related diseases; hypersensitivitypneumonitis; lung fibrosis, including cryptogenic fibrosing alveolitis,idiopathic interstitial pneumonias, fibrosis complicatinganti-neoplastic therapy and chronic infection, including tuberculosisand aspergillosis and other fungal infections; complications of lungtransplantation; vasculitic and thrombotic disorders of the lungvasculature, and pulmonary hypertension; antitussive activity includingtreatment of chronic cough associated with inflammatory and secretoryconditions of the airways, and iatrogenic cough; acute and chronicrhinitis including rhinitis medicamentosa, and vasomotor rhinitis;perennial and seasonal allergic rhinitis including rhinitis nervosa (hayfever); nasal polyposis; acute viral infection including the commoncold, and infection due to respiratory syncytial virus, influenza,coronavirus (including SARS) or adenovirus; or eosinophilic esophagitis;2. bone and joints: arthritides associated with or includingosteoarthritis/osteoarthrosis, both primary and secondary to, forexample, congenital hip dysplasia; cervical and lumbar spondylitis, andlow back and neck pain; osteoporosis, rheumatoid arthritis and Still'sdisease; seronegative spondyloarthropathies including ankylosingspondylitis, psoriatic arthritis, reactive arthritis andundifferentiated spondarthropathy; septic arthritis and otherinfection-related arthopathies and bone disorders such as tuberculosis,including Potts' disease and Poncet's syndrome; acute and chroniccrystal-induced synovitis including urate gout, calcium pyrophosphatedeposition disease, and calcium apatite related tendon, bursal andsynovial inflammation; Behcet's disease; primary and secondary Sjogren'ssyndrome; systemic sclerosis and limited scleroderma; systemic lupuserythematosus, mixed connective tissue disease, and undifferentiatedconnective tissue disease; inflammatory myopathies includingdermatomyositits and polymyositis; polymalgia rheumatica; juvenilearthritis including idiopathic inflammatory arthritides of whateverjoint distribution and associated syndromes, and rheumatic fever and itssystemic complications; vasculitides including giant cell arteritis,Takayasu's arteritis, Churg-Strauss syndrome, polyarteritis nodosa,microscopic polyarteritis, and vasculitides associated with viralinfection, hypersensitivity reactions, cryoglobulins, and paraproteins;low back pain; Familial Mediterranean fever, Muckle-Wells syndrome, andFamilial Hibernian Fever, Kikuchi disease; drug-induced arthalgias,tendonititides, and myopathies;3. pain and connective tissue remodelling of musculoskeletal disordersdue to injury [for example sports injury] or disease: arthritides (forexample rheumatoid arthritis, osteoarthritis, gout or crystalarthropathy), other joint disease (such as intervertebral discdegeneration or temporomandibular joint degeneration), bone remodellingdisease (such as osteoporosis, Paget's disease or osteonecrosis),polychondritits, scleroderma, mixed connective tissue disorder,spondyloarthropathies or periodontal disease (such as periodontitis);4. skin: psoriasis, atopic dermatitis, contact dermatitis or othereczematous dermatoses, and delayed-type hypersensitivity reactions;phyto- and photodermatitis; seborrhoeic dermatitis, dermatitisherpetiformis, lichen planus, lichen sclerosus et atrophica, pyodermagangrenosum, skin sarcoid, discoid lupus erythematosus, pemphigus,pemphigoid, epidermolysis bullosa, urticaria, angioedema, vasculitides,toxic erythemas, cutaneous eosinophilias, alopecia greata, male-patternbaldness, Sweet's syndrome, Weber-Christian syndrome, erythemamultiforme; cellulitis, both infective and non-infective; panniculitis;cutaneous lymphomas, non-melanoma skin cancer and other dysplasticlesions; drug-induced disorders including fixed drug eruptions;5. eyes: blepharitis; conjunctivitis, including perennial and vernalallergic conjunctivitis; iritis; anterior and posterior uveitis;choroiditis; autoimmune; degenerative or inflammatory disordersaffecting the retina; ophthalmitis including sympathetic ophthalmitis;sarcoidosis; infections including viral, fungal, and bacterial;6. gastrointestinal tract: glossitis, gingivitis, periodontitis;oesophagitis, including reflux; eosinophilic gastro-enteritis,mastocytosis, Crohn's disease, colitis (including ulcerative colitis,microscopic colitis and indeterminant colitis), proctitis, pruritis ani;coeliac disease, irritable bowel syndrome, irritable bowel disorder,non-inflammatory diarrhoea, and food-related allergies which may haveeffects remote from the gut (for example migraine, rhinitis or eczema);7. abdominal: hepatitis, including autoimmune, alcoholic and viral;fibrosis and cirrhosis of the liver; cholecystitis; pancreatitis, bothacute and chronic;8. genitourinary: nephritis including interstitial andglomerulonephritis; nephrotic syndrome; cystitis including acute andchronic (interstitial) cystitis and Hunner's ulcer; acute and chronicurethritis, prostatitis, epididymitis, oophoritis and salpingitis;vulvo-vaginitis; Peyronie's disease; erectile dysfunction (both male andfemale);9. allograft rejection: acute and chronic following, for example,transplantation of kidney, heart, liver, lung, bone marrow, skin orcornea or following blood transfusion; or chronic graft versus hostdisease;10. CNS: Alzheimer's disease and other dementing disorders including CJDand nvCJD; amyloidosis; multiple sclerosis and other demyelinatingsyndromes; cerebral atherosclerosis and vasculitis; temporal arteritis;myasthenia gravis; acute and chronic pain (acute, intermittent orpersistent, whether of central or peripheral origin) including visceralpain, headache, migraine, trigeminal neuralgia, atypical facial pain,joint and bone pain, pain arising from cancer and tumour invasion,neuropathic pain syndromes including diabetic, post-herpetic, andHIV-associated neuropathies; neurosarcoidosis; central and peripheralnervous system complications of malignant, infectious or autoimmuneprocesses;11. other auto-immune and allergic disorders including Hashimoto'sthyroiditis, Graves' disease, Addison's disease, diabetes mellitus,idiopathic thrombocytopaenic purpura, eosinophilic fasciitis, hyper-IgEsyndrome, antiphospholipid syndrome;12. other disorders with an inflammatory or immunological component;including acquired immune deficiency syndrome (AIDS), leprosy, Sezarysyndrome, and paraneoplastic syndromes;13. cardiovascular: atherosclerosis, affecting the coronary andperipheral circulation; pericarditis; myocarditis, inflammatory andauto-immune cardiomyopathies including myocardial sarcoid; ischaemicreperfusion injuries; endocarditis, valvulitis, and aortitis includinginfective (for example syphilitic); vasculitides; disorders of theproximal and peripheral veins including phlebitis and thrombosis,including deep vein thrombosis and complications of varicose veins; or,14. oncology: treatment of common cancers including prostate, breast,lung, ovarian, pancreatic, bowel and colon, stomach, skin and braintumours and malignancies affecting the bone marrow (including theleukaemias) and lymphoproliferative systems, such as Hodgkin's andnon-Hodgkin's lymphoma; including the prevention and treatment ofmetastatic disease and tumour recurrences, and paraneoplastic syndromes;in a mammal (for example man).

In a further aspect the invention provides a compound of the invention,or a pharmaceutically acceptable salt thereof, for use in the treatmentof asthma {such as bronchial, allergic, intrinsic, extrinsic or dustasthma, particularly chronic or inveterate asthma (for example lateasthma or airways hyper-responsiveness)}; or rhinitis {including acute,allergic, atrophic or chronic rhinitis, such as rhinitis caseosa,hypertrophic rhinitis, rhinitis purulenta, rhinitis sicca or rhinitismedicamentosa; membranous rhinitis including croupous, fibrinous orpseudomembranous rhinitis or scrofulous rhinitis; seasonal rhinitisincluding rhinitis nervosa (hay fever) or vasomotor rhinitis}.

In a still further aspect a compound of the invention, or apharmaceutically acceptable salt thereof, is useful in the treatment ofasthma.

In another aspect a compound of the invention, or a pharmaceuticallyacceptable salt thereof, is useful in the treatment of respiratorysyncytial virus (RSV).

The present invention also provides a the use of a compound of theinvention, or a pharmaceutically acceptable salt thereof, in themanufacture of a medicament for use in the treatment of asthma {such asbronchial, allergic, intrinsic, extrinsic or dust asthma, particularlychronic or inveterate asthma (for example late asthma or airwayshyper-responsiveness)}; or rhinitis {including acute, allergic, atrophicor chronic rhinitis, such as rhinitis caseosa, hypertrophic rhinitis,rhinitis purulenta, rhinitis sicca or rhinitis medicamentosa; membranousrhinitis including croupous, fibrinous or pseudomembranous rhinitis orscrofulous rhinitis; seasonal rhinitis including rhinitis nervosa (hayfever) or vasomotor rhinitis}.

In order to use a compound of formula (I), or a pharmaceuticallyacceptable salt thereof, for the therapeutic treatment of a mammal, suchas man, said ingredient is normally formulated in accordance withstandard pharmaceutical practice as a pharmaceutical composition.Therefore in another aspect the present invention provides apharmaceutical composition which comprises a compound of formula (I), ora pharmaceutically acceptable salt thereof (active ingredient), and apharmaceutically acceptable adjuvant, diluent or carrier.

In a further aspect the present invention provides a process for thepreparation of said composition which comprises mixing active ingredientwith a pharmaceutically acceptable adjuvant, diluent or carrier.Depending on the mode of administration, the pharmaceutical compositionwill, for example, comprise from 0.05 to 99% w (percent by weight), suchas from 0.05 to 80% w, for example from 0.10 to 70% w, such as from 0.10to 50% w, of active ingredient, all percentages by weight being based ontotal composition.

The pharmaceutical compositions comprising a compound of formula (I), ora pharmaceutically acceptable salt thereof, may be administered instandard manner for the disease condition that it is desired to treat,for example by topical (such as to the lung and/or airways or to theskin), oral, rectal or parenteral (such as intravenous, sub-cutaneous,intramuscular or intra-articular) administration. For these purposes thecompounds of this invention may be formulated by means known in the art.A suitable pharmaceutical composition of this invention is one suitablefor oral administration in unit dosage form, for example a tablet orcapsule which contains between 0.1 mg and 1 g of active ingredient.

Each patient may receive, for example, a dose of 0.01 mgkg⁻¹ to 100mgkg⁻¹, for example in the range of 0.1 mgkg⁻¹ to 20 mgkg⁻¹, of theactive ingredient administered, for example, 1 to 4 times per day.

The invention further relates to a combination therapy wherein acompound of formula (I), or a pharmaceutically acceptable salt thereof,or a pharmaceutical composition or formulation comprising a compound ofthe invention, is administered concurrently or sequentially or as acombined preparation with another therapeutic agent or agents, for thetreatment of one or more of the conditions listed.

In particular, for the treatment of the inflammatory diseases such as(but not restricted to) rheumatoid arthritis, osteoarthritis, asthma,allergic rhinitis, chronic obstructive pulmonary disease (COPD),psoriasis, and inflammatory bowel disease, the compounds of theinvention may be combined with agents listed below.

Non-steroidal anti-inflammatory agents (hereinafter NSAIDs) includingnon-selective cyclo-oxygenase COX-1/COX-2 inhibitors whether appliedtopically or systemically (such as piroxicam, diclofenac, propionicacids such as naproxen, flurbiprofen, fenoprofen, ketoprofen andibuprofen, fenamates such as mefenamic acid, indomethacin, sulindac,azapropazone, pyrazolones such as phenylbutazone, salicylates such asaspirin); selective COX-2 inhibitors (such as meloxicam, celecoxib,rofecoxib, valdecoxib, lumarocoxib, parecoxib and etoricoxib);cyclo-oxygenase inhibiting nitric oxide donors (CINODs);glucocorticosteroids (whether administered by topical, oral,intramuscular, intravenous, or intra-articular routes); methotrexate;leflunomide; hydroxychloroquine; d-penicillamine; auranofin or otherparenteral or oral gold preparations; analgesics; diacerein;intra-articular therapies such as hyaluronic acid derivatives; andnutritional supplements such as glucosamine.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, together with a cytokine or agonist or antagonist of cytokinefunction, (including agents which act on cytokine signalling pathwayssuch as modulators of the SOCS system) including alpha-, beta-, andgamma-interferons; insulin-like growth factor type I (IGF-1);interleukins (IL) including IL1 to 17, and interleukin antagonists orinhibitors such as anakinra; tumour necrosis factor alpha (TNF-a)inhibitors such as anti-TNF monoclonal antibodies (for exampleinfliximab; adalimumab, and CDP-870) and TNF receptor antagonistsincluding immunoglobulin molecules (such as etanercept) andlow-molecular-weight agents such as pentoxyfylline.

In addition the invention relates to a combination of a compound of theinvention, or a pharmaceutically acceptable salt thereof, with amonoclonal antibody targeting B-Lymphocytes (such as CD20 (rituximab),MRA-aIL16R) or T-Lymphocytes (such as CTLA4-Ig, HuMax I1-15).

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, with a modulator of chemokine receptor function such as anantagonist of CCR1, CCR2, CCR2A, CCR2B, CCR3, CCR4, CCR5, CCR6, CCR7,CCR8, CCR9, CCR10 and CCR11 (for the C-C family); CXCR1, CXCR2, CXCR3,CXCR4 and CXCR5 (for the C-X-C family) and CX₃CR1 for the C-X₃-C family.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, with aninhibitor of matrix metalloprotease (MMPs), i.e., the stromelysins, thecollagenases, and the gelatinases, as well as aggrecanase; for examplecollagenase-1 (MMP-1), collagenase-2 (MMP-8), collagenase-3 (MMP-13),stromelysin-1 (MMP-3), stromelysin-2 (MMP-10), and stromelysin-3(MMP-11) and MMP-9 and MMP-12, including agents such as doxycycline.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and a leukotriene biosynthesis inhibitor, 5-lipoxygenase (5-LO)inhibitor or 5-lipoxygenase activating protein (FLAP) antagonist suchas; zileuton; ABT-761; fenleuton; tepoxalin; Abbott-79175; Abbott-85761;a N-(5-substituted)-thiophene-2-alkylsulfonamide;2,6-di-tert-butylphenolhydrazones; a methoxytetrahydropyran such asZeneca ZD-2138; the compound SB-210661; a pyridinyl-substituted2-cyanonaphthalene compound such as L-739,010; a 2-cyanoquinolinecompound such as L-746,530; or an indole or quinoline compound such asMK-591, MK-886, and BAY x 1005.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, and areceptor antagonist for leukotrienes (LT) B4, LTC4, LTD4, and LTE4.selected from the group consisting of the phenothiazin-3-yls such asL-651,392; amidino compounds such as CGS-25019c; benzoxalamines such asontazolast; benzenecarboximidamides such as BIIL 284/260; and compoundssuch as zafirlukast, ablukast, montelukast, pranlukast, verlukast(MK-679), RG-12525, Ro-245913, iralukast (CGP 45715A), and BAY x 7195.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and a phosphodiesterase (PDE) inhibitor such as amethylxanthanine including theophylline and aminophylline; a selectivePDE isoenzyme inhibitor including a PDE4 inhibitor, an inhibitor of theisoform PDE4D, or an inhibitor of PDE5.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, and ahistamine type 1 receptor antagonist such as cetirizine, levocetirizine,loratadine, desloratadine, fexofenadine, acrivastine, terfenadine,astemizole, azelastine, levocabastine, chlorpheniramine, promethazine,cyclizine, or mizolastine; applied orally, topically or parenterally.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and a proton pump inhibitor (such as omeprazole) or agastroprotective histamine type 2 receptor antagonist.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, and anantagonist of the histamine type 4 receptor.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and an alpha-1/alpha-2 adrenoceptor agonist vasoconstrictorsympathomimetic agent, such as propylhexedrine, phenylephrine,phenylpropanolamine, ephedrine, pseudoephedrine, naphazolinehydrochloride, oxymetazoline hydrochloride, tetrahydrozolinehydrochloride, xylometazoline hydrochloride, tramazoline hydrochlorideor ethylnorepinephrine hydrochloride.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, and ananticholinergic agent including muscarinic receptor (M1, M2, and M3)antagonist such as atropine, hyoscine, glycopyrrrolate, ipratropiumbromide, tiotropium bromide, oxitropium bromide, pirenzepine ortelenzepine.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and a beta-adrenoceptor agonist (including beta receptorsubtypes 1-4) such as isoprenaline, salbutamol, formoterol, salmeterol,terbutaline, orciprenaline, bitolterol mesylate, or pirbuterol, or achiral enantiomer thereof.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, and achromone, such as sodium cromoglycate or nedocromil sodium.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, with a glucocorticoid, such as flunisolide, triamcinoloneacetonide, beclomethasone dipropionate, budesonide, fluticasonepropionate, ciclesonide or mometasone furoate.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, with anagent that modulates a nuclear hormone receptor such as PPARs.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, together with an immunoglobulin (Ig) or Ig preparation or anantagonist or antibody modulating Ig function such as anti-IgE (forexample omalizumab).

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, andanother systemic or topically-applied anti-inflammatory agent, such asthalidomide or a derivative thereof, a retinoid, dithranol orcalcipotriol.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and combinations of aminosalicylates and sulfapyridine such assulfasalazine, mesalazine, balsalazide, and olsalazine; andimmunomodulatory agents such as the thiopurines, and corticosteroidssuch as budesonide.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof,together with an antibacterial agent such as a penicillin derivative, atetracycline, a macrolide, a beta-lactam, a fluoroquinolone,metronidazole, an inhaled aminoglycoside; an antiviral agent includingacyclovir, famciclovir, valaciclovir, ganciclovir, cidofovir,amantadine, rimantadine, ribavirin, zanamavir and oseltamavir; aprotease inhibitor such as indinavir, nelfinavir, ritonavir, andsaquinavir; a nucleoside reverse transcriptase inhibitor such asdidanosine, lamivudine, stavudine, zalcitabine or zidovudine; or anon-nucleoside reverse transcriptase inhibitor such as nevirapine orefavirenz.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and a cardiovascular agent such as a calcium channel blocker, abeta-adrenoceptor blocker, an angiotensin-converting enzyme (ACE)inhibitor, an angiotensin-2 receptor antagonist; a lipid lowering agentsuch as a statin or a fibrate; a modulator of blood cell morphology suchas pentoxyfylline; thrombolytic, or an anticoagulant such as a plateletaggregation inhibitor.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof, and aCNS agent such as an antidepressant (such as sertraline), ananti-Parkinsonian drug (such as deprenyl, L-dopa, ropinirole,pramipexole, a MAOB inhibitor such as selegine and rasagiline, a comPinhibitor such as tasmar, an A-2 inhibitor, a dopamine reuptakeinhibitor, an NMDA antagonist, a nicotine agonist, a dopamine agonist oran inhibitor of neuronal nitric oxide synthase), or an anti-Alzheimer'sdrug such as donepezil, rivastigmine, tacrine, a COX-2 inhibitor,propentofylline or metrifonate.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, and an agent for the treatment of acute or chronic pain, suchas a centrally or peripherally-acting analgesic (for example an opioidor derivative thereof), carbamazepine, phenyloin, sodium valproate,amitryptiline or other anti-depressant agents, paracetamol, or anon-steroidal anti-inflammatory agent.

The present invention further relates to the combination of a compoundof the invention, or a pharmaceutically acceptable salt thereof,together with a parenterally or topically-applied (including inhaled)local anaesthetic agent such as lignocaine or a derivative thereof.

A compound of the present invention, or a pharmaceutically acceptablesalt thereof, can also be used in combination with an anti-osteoporosisagent including a hormonal agent such as raloxifene, or a biphosphonatesuch as alendronate.

The present invention still further relates to the combination of acompound of the invention, or a pharmaceutically acceptable saltthereof, together with a: (i) tryptase inhibitor; (ii) plateletactivating factor (PAF) antagonist; (iii) interleukin converting enzyme(ICE) inhibitor; (iv) IMPDH inhibitor; (v) adhesion molecule inhibitorsincluding VLA-4 antagonist; (vi) a cathepsin; (vii) kinase inhibitorsuch as an inhibitor of tyrosine kinase (such as Btk, Itk, Jak3 or MAP,for example Gefitinib or Imatinib mesylate), a serine/threonine kinase(such as an inhibitor of a MAP kinase such as p38, JNK, protein kinaseA, B or C, or IKK), or a kinase involved in cell cycle regulation (suchas a cylin dependent kinase); (viii) glucose-6 phosphate dehydrogenaseinhibitor; (ix) kinin-B.sub1.- or B.sub2.-receptor antagonist; (x)anti-gout agent, for example colchicine; (xi) xanthine oxidaseinhibitor, for example allopurinol; (xii) uricosuric agent, for exampleprobenecid, sulfinpyrazone or benzbromarone; (xiii) growth hormonesecretagogue; (xiv) transforming growth factor (TGFβ); (xv)platelet-derived growth factor (PDGF); (xvi) fibroblast growth factorfor example basic fibroblast growth factor (bFGF); (xvii) granulocytemacrophage colony stimulating factor (GM-C SF); (xviii) capsaicin cream;(xix) tachykinin NK.sub1. or NK.sub3. receptor antagonist such asNKP-608C, SB-233412 (talnetant) or D-4418; (xx) elastase inhibitor suchas UT-77 or ZD-0892; (xxi) TNF-alpha converting enzyme inhibitor (TACE);(xxii) induced nitric oxide synthase (iNOS) inhibitor; (xxiii)chemoattractant receptor-homologous molecule expressed on TH2 cells,(such as a CRTH2 antagonist); (xxiv) inhibitor of p38; (xxv) agentmodulating the function of Toll-like receptors (TLR), (xxvi) agentmodulating the activity of purinergic receptors such as P2×7; (xxvii)inhibitor of transcription factor activation such as NFkB, API, orSTATS; or (xxviii) a non-steroidal glucocorticoid receptor agonist.

In particular a compound of formula (I), or a pharmaceuticallyacceptable salt thereof, can be combined with a histamine type 1receptor antagonist such as cetirizine, levocitirizine, loratadine,desloratadine, fexofenadine, acrivistine, azelastine, levocabastine,chlorpheniramine, promethazine, cyclizine or mizolastine; appliedorally, topically or parenterally (for example orally).

A compound of the invention, or a pharmaceutically acceptable saltthereof, can also be used in combination with an existing therapeuticagent for the treatment of cancer, for example suitable agents include:

(i) an antiproliferative/antineoplastic drug or a combination thereof,as used in medical oncology, such as an alkylating agent (for examplecis-platin, carboplatin, cyclophosphamide, nitrogen mustard, melphalan,chlorambucil, busulphan or a nitrosourea); an antimetabolite (forexample an antifolate such as a fluoropyrimidine like 5-fluorouracil ortegafur, raltitrexed, methotrexate, cytosine arabinoside, hydroxyurea,gemcitabine or paclitaxel); an antitumour antibiotic (for example ananthracycline such as adriamycin, bleomycin, doxorubicin, daunomycin,epirubicin, idarubicin, mitomycin-C, dactinomycin or mithramycin); anantimitotic agent (for example a vinca alkaloid such as vincristine,vinblastine, vindesine or vinorelbine, or a taxoid such as taxol ortaxotere); or a topoisomerase inhibitor (for example anepipodophyllotoxin such as etoposide, teniposide, amsacrine, topotecanor a camptothecin);(ii) a cytostatic agent such as an antioestrogen (for example tamoxifen,toremifene, raloxifene, droloxifene or iodoxyfene), an oestrogenreceptor down regulator (for example fulvestrant), an antiandrogen (forexample bicalutamide, flutamide, nilutamide or cyproterone acetate), aLHRH antagonist or LHRH agonist (for example goserelin, leuprorelin orbuserelin), a progestogen (for example megestrol acetate), an aromataseinhibitor (for example as anastrozole, letrozole, vorazole orexemestane) or an inhibitor of 5α-reductase such as finasteride;(iii) an agent which inhibits cancer cell invasion (for example ametalloproteinase inhibitor like marimastat or an inhibitor of urokinaseplasminogen activator receptor function); (iv) an inhibitor of growthfactor function, for example: a growth factor antibody (for example theanti-erb b2 antibody trastuzumab, or the anti-erb b1 antibody cetuximab[C225]), a farnesyl transferase inhibitor, a tyrosine kinase inhibitoror a serine/threonine kinase inhibitor, an inhibitor of the epidermalgrowth factor family (for example an EGFR family tyrosine kinaseinhibitor such asN-(3-chloro-4-fluorophenyl)-7-methoxy-6-(3-morpholinopropoxy)quinazolin-4-amine(gefitinib, AZD1839),N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine(erlotinib, OSI-774) or6-acrylamido-N-(3-chloro-4-fluorophenyl)-7-(3-morpholinopropoxy)quinazolin-4-amine(CI 1033)), an inhibitor of the platelet-derived growth factor family,or an inhibitor of the hepatocyte growth factor family;(v) an antiangiogenic agent such as one which inhibits the effects ofvascular endothelial growth factor (for example the anti-vascularendothelial cell growth factor antibody bevacizumab, a compounddisclosed in WO 97/22596, WO 97/30035, WO 97/32856 or WO 98/13354), or acompound that works by another mechanism (for example linomide, aninhibitor of integrin αvβ3 function or an angiostatin);(vi) a vascular damaging agent such as combretastatin A4, or a compounddisclosed in WO 99/02166, WO 00/40529, WO 00/41669, WO 01/92224, WO02/04434 or WO 02/08213;(vii) an agent used in antisense therapy, for example one directed toone of the targets listed above, such as ISIS 2503, an anti-rasantisense;(viii) an agent used in a gene therapy approach, for example approachesto replace aberrant genes such as aberrant p53 or aberrant BRCA1 orBRCA2, GDEPT (gene-directed enzyme pro-drug therapy) approaches such asthose using cytosine deaminase, thymidine kinase or a bacterialnitroreductase enzyme and approaches to increase patient tolerance tochemotherapy or radiotherapy such as multi-drug resistance gene therapy;or,(ix) an agent used in an immunotherapeutic approach, for example ex-vivoand in-vivo approaches to increase the immunogenicity of patient tumourcells, such as transfection with cytokines such as interleukin 2,interleukin 4 or granulocyte-macrophage colony stimulating factor,approaches to decrease T-cell anergy, approaches using transfectedimmune cells such as cytokine-transfected dendritic cells, approachesusing cytokine-transfected tumour cell lines and approaches usinganti-idiotypic antibodies.

The invention will now be illustrated by the following non-limitingexamples in which, unless stated otherwise:

(i) when given, ¹H NMR data is quoted and is in the form of delta valuesfor major diagnostic protons, given in parts per million (ppm) relativeto tetramethylsilane (TMS) as an internal standard, determined at 300MHz or 400 MHz using perdeuterio DMSO-D6 (CD₃SOCD₃) or CDCl₃ as thesolvent unless otherwise stated;(ii) mass spectra (MS) were run with an electron energy of 70 electronvolts in the chemical ionisation (CI) mode using a direct exposureprobe; where indicated ionisation was effected by electron impact (EI)or fast atom bombardment (FAB); where values for m/z are given,generally only ions which indicate the parent mass are reported, andunless otherwise stated the mass ion quoted is the positive massion—(M+H)';(iii) the title and sub-title compounds of the examples and methods werenamed using either the name program from Advanced Chemistry DevelopmentInc, version 6.00; or the index name program from Ogham with thestereochemical descriptors being added by hand (seewww.eyesopen.com/products/applications/ogham.html);(iv) unless stated otherwise, reverse phase HPLC was conducted using a“Symmetry”, “NovaPak” or “Xterra” reverse phase silica column, allavailable from Waters Corp.;(v) for analytical HPLC the following conditions were used:Reverse phase analytical HPLC (Hewlett Packard Series 1100) using Waters“Symmetry” C8 column 3.5 μm; 4.6×50 mm column using 0.1% ammoniumacetate/acetonitrilegradients at 2 mL/min given as % aqueousSTANDARD 75% to 5% over 3 minFAST 45% to 5% over 2.5 min

MEDIUM FAST 65% to 5% in 2.5 min SLOW 95% to 50% in 2.5 min

SUPERSLOW 100% to 80% in 2.5 min;

(vi) Method for X-Ray Powder Diffractometry (XRPD)

Analyses were performed on a Siemens model D5000 fitted with a positionsensitive detector (PSD), a Philips X′ pert Pro fitted with an X′celerator detector or a Rigaku MiniFlex X-ray powder diffractometerfitted with a scintillation detector. Samples (1-2 mg) were sprinkled ona silicon wafer zero-background holder and irradiated with copper K_(α)radiation (λ=1.54056 Å). Reflections were collected between2.017-39.967° 2θ, typically at a step size of 0.033° 2θ. Otherparameters for these analyses were:

-   -   Generator=45 kV 40 mA    -   Scan time ˜30 min    -   Measured time/step=200.025 sec    -   Divergence slit fixed=1.0    -   Scan axis=Gonio    -   PSD length=2.122    -   PSD mode=scanning    -   Incident beam monochromator    -   Sample=spinning        and        (v) the following abbreviations are used:

RPHPLC Reverse phase high pressure liquid chromatography min minutesDMEM tissue culture medium Dulbecco's Modified Eagles Medium PSG acombination of penicillin, streptomycin and L-glutamine FCS foetal calfserum NEAA Non-essential amino acids h hour THF Tetrahydrofuran LC/MSHPLC coupled with mass spectrometry SCX Strong cation exchange resin(Isolute SCX-2)

PREPARATION 12-Chloro-4-({1-[(3,4-dihydroxycyclopentyl)methyl]piperidin-4-yl}oxy)-3-methylbenzonitrileA2-Chloro-4-{[1-(cyclopent-3-en-1-ylmethyl)piperidin-4-yl]oxy}-3-methylbenzonitrile

2-Chloro-3-methyl-4-(piperidin-4-yloxy)benzonitrile (1.3 g) and aceticacid (0.32 ml) were combined in THF (20 ml). Sodiumtriacetoxyborohydride was added (1.4 g) followed bycyclopent-3-ene-1-carbaldehyde (0.62 g). The reaction was stirred for 1h and then concentrated. The residue was partitioned between aqueoussodium bicarbonate solution and dichloromethane. The organic phase waswashed with brine, dried, filtered and evaporated. The residue waspurified by chromatography eluting with ethyl acetate to give thesubtitle compound (1.5 g).

¹H NMR δ_((CDCl3)): 1.78-1.90 (2H, m), 1.93-2.14 (4H, m), 2.28-2.39 (7H,m), 2.41-2.53 (3H, m), 2.63-2.72 (2H, m), 4.38-4.48 (1H, m), 5.64 (2H,s), 6.79 (1H, d), 7.46 (1H, d).

MS (ES+ve) 331/333 (M+H)+

Retention time (standard) 2.66

B2-Chloro-4-({1-[(3,4-dihydroxycyclopentyl)methyl]piperidin-4-yl}oxy)-3-methylbenzonitrile

2-Chloro-4-(1-cyclopent-3-enylmethyl-piperidin-4-yloxy)-3-methyl-benzonitrile(1.5 g), potassium osmate (vi) dihydrate (0.042 g) and4-methylmorpholine 4-oxide monohydrate (3.2 ml of a 50% soln in water)were added to acetone (40 ml) and water (5 ml). The reaction mixture washeated under reflux for 1 h. LC/MS showed complete conversion to thedesired diol. The reaction was allowed to cool to room temperature andthen sodium metabisulfite solution was added. The reaction mixture wasextracted with dichloromethane, then sodium bicarbonate solution wasadded and the aqueous mixture was extracted again with dichloromethane.The organic extracts were combined and evaporated. The residue wasloaded onto an SCX cartridge and eluted with dichloromethane/methanoland then with 0.7M ammonia in methanol to give the title compound (1.3g).

¹H NMR δ_((CDCl3)): 1.42-1.64 (2H, m), 1.78-2.14 (4H, m), 2.23-2.47 (9H,m), 2.51-2.86 (4H, m), 3.72 (1H, t), 3.92-4.18 (2H, m), 4.38-4.50 (1H,m), 6.78 (1H, d), 7.46 (1H, d).

MS (ES+ve) 365/367 (M+H)+

Retention time (standard) 1.53

INTERMEDIATE 1

This illustrates the preparation of methyl2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoate

4-[4-(3,4-Dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-cyclopentane-1,2-diol(0.50 g) was stirred with acetic acid (0.077 ml) in water until itdissolved. Sodium periodate (0.286 g) was added and the reaction mixturewas stirred, under nitrogen, for 15 min. The reaction mixture wasneutralised by addition of potassium carbonate (240 mg) and product wasextracted with dichloromethane. The dichloromethane was washed withbrine, dried (MgSO₄), and filtered into a reaction flask containing2-amino-3-(4-fluoro-phenyl)-propionic acid methyl ester (0.312 g),sodium triacetoxy borohydride (0.651 g) and acetic acid (0.077 ml) indichloromethane (10 ml). The mixture was stirred at room temperature for1 h. A saturated solution of sodium bicarbonate was added and productwas extracted with dichloromethane. The dichloromethane was washed withbrine, dried (MgSO₄), filtered and concentrated. Crude product waspurified by flash chromatography eluting with ethyl acetate to give thetitle compound (0.52 g).

¹H NMR δ_((CDCL3)): 1.08-1.29 (m, 2H), 1.41-1.63 (m, 1H), 1.69-1.86 (m,4H), 1.90-2.00 (m, 2H), 2.14-2.39 (m, 9H), 2.57-2.68 (m, 2H), 2.82-2.95(m, 2H), 2.97-3.09 (m, 2H), 3.39 (dd, 1H), 3.59 (s, 3H), 4.22-4.33 (m,1H), 6.71 (d, 1H), 6.90-7.03 (m, 2H), 7.11-7.23 (m, 3H).

The following Intermediates were prepared analogously from theappropriate amino esters and diols (diols not previously described wereprepared analogously to WO2004087659):

MS Retention Inter- [M + H]⁺ time (fast mediate Name (ES+) gradient) ¹HNMR δ_((CD3OD)) 2 Methyl (2S)-2-[4-[[4- 2.41 (3,4-dichloro-2-methyl-phenoxy)-1- piperidyl]methyl]-1- piperidyl]-3-(2- methoxyphenyl)-propanoate 3 Methyl (2S)-3-(4- 0.97-1.14 (m, 2H), 1.37-cyanophenyl)-2-[4-[[4- 1.52 (m, 1H), 1.58-1.76 (3,4-dichloro-2-methyl-(m, 4H), 1.84-1.95 (m, phenoxy)-1- 2H), 2.10-2.15 (m, 2H),piperidyl]methyl]-1- 2.16-2.39 (m, 7H), 2.53- piperidyl]-propanoate 2.63(m, 2H), 2.73-2.81 (m, 1H), 2.89-2.99 (m, 3H), 3.35-3.42 (m, 1H), 3.50(s, 3H), 4.27-4.37 (m, 1H), 6.81 (d, 1H), 7.17 (d, 1H), 7.30 (d, 2H),7.53 (d, 2H) 4 Methyl (2S)-2-(4-{[4- 537/539 2.23 (3,4-dichlorophenoxy)-piperidin-1- yl]methyl}piperidin-1- yl)-3-(4-fluorophenyl)-2-methylpropanoate 5 Methyl (2S)-2-[4-[[4-(4- 517/519 2.20chloro-2-methyl- phenoxy)-1- piperidyl]methyl]-1- piperidyl]-3-(4-fluorophenyl)-2-methyl- propanoate 6 Methyl (2S)-2-[4-[[4- 551/553 2.54(3,4-dichloro-2-methyl- phenoxy)-1- piperidyl]methyl]-1-piperidyl]-3-(4- fluorophenyl)-2-methyl- propanoate 7 (±)-Methyl2-[4-[[4- 519/521 2.24 (3,4-dichlorophenoxy)- 1-piperidyl]methyl]-1-piperidyl]-2-methyl-3- phenyl-propanoate 10 (±)-Methyl 2-[4-[[4- 533/5352.69 (3,4-dichloro-2-methyl- phenoxy)-1- piperidyl]methyl]-1-piperidyl]-2-methyl-3- phenyl-propanoate 13 Methyl (2S)-2-[4-[[4-533/535 2.66 (3,4-dichloro-2-ethyl- phenoxy)-1- piperidyl]methyl]-1-piperidyl]-3- phenylpropanoate 14 Methyl (2S)-2-[4-[[4- 551/553 2.71(3,4-dichloro-2-ethyl- phenoxy)-1- piperidyl]methyl]-1- piperidyl]-3-(4-fluorophenyl)- propanoate 15 Methyl (2S)-2-(4-{[4-(3- 1.14-1.33 (2H, m),1.50- chloro-4-cyano-2- 1.65 (1H, m), 1.74-1.92 methylphenoxy)- (4H, m),2.00-2.11 (2H, piperidin-1- m), 2.24-2.30 (3H, m),yl]methyl}piperidin-1- 2.33 (3H, s), 2.36-2.46 yl)-3-phenylpropanoate(3H, m), 2.64-2.74 (2H, m), 2.94-3.10 (4H, m), 3.45 (1H, dd), 3.57 (3H,s), 4.58-4.66 (1H, m), 7.09 (1H, d), 7.16-7.30 (5H, m), 7.61 (1H, d) 16Methyl (2S)-2-(4-{[4-(3- 2.82 1.08-1.29 (m, 2H), 1.41- chloro-4-cyano-2-(standard 1.63 (m, 1H), 1.69-1.86 methylphenoxy)- gradient) (m, 4H),1.90-2.00 (m, piperidin-1- 2H), 2.14-2.39 (m, 9H),yl]methyl}piperidin-1- 2.57-2.68 (m, 2H), 2.82- yl)-3-(4- 2.95 (m, 2H),2.97-3.09 fluorophenyl)propanoate (m, 2H), 3.39 (dd, 1H), 3.59 (s, 3H),4.22-4.33 (m, 1H), 6.71 (d, 1H), 6.90- 7.03 (m, 2H), 7.11-7.23 (m, 3H)17 Methyl (2S)-2-[4-[[4- 537/539 1.12-1.32 (2H, m), 1.49-(2,4-dichloro-3-methyl- 1.64 (1H, m), 1.73-1.92 phenoxy)-1- (4H, m),1.95-2.06 (2H, piperidyl]methyl]-1- m), 2.25 (2H, d), 2.30-piperidyl]-3-(4- 2.43 (3H, m), 2.47 (3H, s), fluorophenyl)- 2.66-2.77(2H, m), 2.89- propanoate 3.06 (4H, m), 3.42 (1H, dd), 3.58 (3H, s),3.67- 3.73 (1H, m), 4.43-4.52 (1H, m), 6.94-7.07 (3H, m), 7.18-7.29 (3H,m) 18 Methyl (2S)-2-[4-[[4-(4- 1.11-1.33 (2H, m), 1.49- chloro-2-methyl-1.66 (1H, m), 1.73-1.88 phenoxy)-1- (4H, m), 1.97-2.07 (2H,piperidyl]methyl]-1- m), 2.20 (3H, s), 2.23- piperidyl]-3-(4- 2.28 (3H,m), 2.30-2.44 fluorophenyl)- (3H, m), 2.66-2.76 (2H, propanoate m),2.91-3.08 (4H, m), 3.39-3.46 (1H, m), 3.58 (3H, s), 4.36-4.44 (1H, m),6.89 (1H, d), 6.96- 7.04 (2H, m), 7.07-7.14 (2H, m), 7.18-7.25 (2H, m)19 Methyl (2S)-2-[4-[[4- 1.12-1.32 (2H, m), 1.49-(2,4-dichloro-phenoxy)- 1.64 (1H, m), 1.73-1.91 1-piperidyl]methyl]-1-(4H, m), 1.95-2.05 (2H, piperidyl]-3-(4- m), 2.22-2.28 (2H, m),fluorophenyl)- 2.30-2.43 (3H, m), 2.67- propanoate 2.77 (2H, m),2.90-3.07 (4H, m), 3.42 (1H, dd), 3.58 (3H, s), 3.69-3.73 (1H, m),4.43-4.53 (1H, m), 6.96-7.11 (3H, m), 7.18-7.27 (3H, m), 7.41 (1H, d)

INTERMEDIATES 8 & 9

This illustrates the preparation of the 2 enantiomers of methyl2-[4-[[4-(3,4-dichlorophenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoate

(±)-Methyl2-[4-[[4-(3,4-dichlorophenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoate(185 mg) was eluted through a Chiralpak AD HPLC column in ethanolcontaining 0.1% diethylamine to give two enantiomers.

Isomer 1 (76 mg) retention time (Chiralpak AD 4.6×250 mm; 0.5 ml/minethanol) 7.68 min.

Isomer 2 (73 mg) retention time (Chiralpak AD 4.6×250 mm; 0.5 ml/minethanol) 9.57 min.

INTERMEDIATES 11 & 12

This illustrates the preparation of the 2 enantiomers of methyl2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoate

These were prepared following the method of Intermediates 8 & 9 using(±)-methyl2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-2-methyl-3-phenyl-propanoateto give two enantiomers.

Isomer 3 retention time (Chiralpak AD 4.6×250 mm; 0.5 ml/min ethanolcontaining 0.1% diethylamine) 12.58 min.

Isomer 4 retention time (Chiralpak AD 4.6×250 mm; 0.5 ml/min ethanolcontaining 0.1% diethylamine) 15.76 min.

INTERMEDIATE 20

This illustrates the preparation of methyl2-benzyl-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)butanoate

This compound was prepared following the method of Example 1 using2-amino-2-benzyl-butyric acid methyl ester and4-[4-(3,4-dichloro-phenoxy)-piperidin-1-ylmethyl]-cyclopentane-1,2-diol.

MS (ESI⁺) 533/535 (M+H⁺)

RT (fast gradient) 2.94 min.

INTERMEDIATE 21

This illustrates the preparation of4-(3,4-dichloro-2-methyl-phenoxy)-piperidine hydrochloride

4-Hydroxypiperidine (32.5 g) and potassium tert-butoxide (62.7 g) wereadded to a 1 L jacketed vessel. Tetrahydrofuran (275 mL) was addedfollowed by N-methylpyrrolidone (25 mL).1,2-Dichloro-4-fluoro-3-methylbenzene (50 g) in tetrahydrofuran (100 mL)was then added, followed by tetrahydrofuran (100 mL). The mixture washeated to 67° C. overnight then cooled to 50° C. Water (250 mL) wasadded and the mixture was stirred for 10 min at 50° C. The layers wereseparated and the heating was removed. The organic layer was washed withtwice with 10% w/w brine (250 mL). The organic layer was heated toremove solvent by distillation firstly at atmospheric pressure and thenunder vacuum (400 mbar) whilst isopropanol (950 mL) was added until thetetrahydrofuran was replaced by isopropanol. The solution was thenheated to 50° C. Hydrogen chloride in isopropanol (5.5M, 125 mL) wasadded, an exotherm to 60° C. was observed and the solution was cooled to50° C. The mixture was cooled from 50° C. to 10° C. over 1 h and thenstirred overnight at 10° C. The product was collected by filtration,washed with isopropanol (50 mL) and dried under vacuum at 40° C. to give4-(3,4-dichloro-2-methyl-phenoxy)-piperidine hydrochloride as anoff-white solid (62.3 g).

¹H NMR δ_((CDCL3)) 2.17 (2H, dd), 2.29-2.39 (2H, m), 2.34 (3H, s), 3.33(4H, dd), 4.61-4.66 (1H, m), 6.68 (1H, d), 7.25 (1H, d), 9.64-9.83 (1H,m).

INTERMEDIATE 22

This illustrates the preparation of4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidine-1-carboxylicacid tert-butyl ester

Acetonitrile (144 mL) and water (336 mL) were added to a mixture of4-(3,4-dichloro-2-methyl-phenoxy)-piperidine hydrochloride (60 g),4-(toluene-4-sulfonyloxymethyl)-piperidine-1-carboxylic acid tert-butylester (74.7 g) and potassium carbonate (57.3 g) and the mixture washeated to reflux for 7 h, then cooled over 30 min to 75° C. and held at75° C. for 14 h, then heated over 30 min to reflux. Acetonitrile (192mL) was added and then the mixture was cooled to 20° C. over 2 h to givea suspension. The suspension was filtered under vacuum, the filter cakewas washed with water (180 mL) and then with acetonitrile (180 mL) anddried under vacuum at 40° C. to give4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidine-1-carboxylicacid tert-butyl ester as a white solid (73.9 g).

¹H NMR δ_((CD3OD)) 0.99-1.12 (2H, m), 1.45 (9H, s), 1.69-1.85 (5H, m),1.95-2.04 (2H, m), 2.23 (2H, d), 2.31 (3H, s), 2.32-2.40 (2H, m),2.64-2.82 (4H, m), 4.05 (2H, d), 4.38-4.46 (1H, m), 6.91 (1H, d), 7.27(1H, d)

INTERMEDIATE 23

This illustrates the preparation of4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidinedi-benzenesulfonate salt

A suspension of4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidine-1-carboxylicacid tert-butyl ester (120 g) and ethanol (600 mL) were heated to 75° C.to give a solution. Benzenesulfonic acid (70% in water, 144.2 g) inethanol (120 mL) was added dropwise over 45 min followed by a rinse withethanol (60 mL). The solution was heated at 75° C. for 1 h and was thencooled to 20° C. over 1 h 45 min. The resultant solid was collected, thefilter cake was washed with ethanol (480 mL) then dried under vacuumovernight at 40° C. to give4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidinedi-benzenesulfonate salt as a white solid (161.9 g).

¹H NMR δ_((DMSO)) 1.3-1.41 (2H, m), 1.89-1.93 (3H, m), 2.02-2.15, (4H,m), 2.25, s and 2.34 (3H, s), 2.83-2.94 (2H, m), 3.06-3.12, (4H, m),3.28-3.36, (2H, m), 3.45-3.49, (1H, m), 3.58-3.62 (1H, m) 4.5-4.65 and4.78-4.84 (2×m, 1H) 7.09 and 7.14 (2×d, 1H), 7.3-7.37, (6H, m), 7.45(1H, d); 7.59-7.63 (4H, m), 8.23 (1H, br s), 8.49 (1H, br s), 8.98 (1H,br s).

INTERMEDIATE 24

This illustrates the preparation of(R)-2-(4-nitro-benzenesulfonyloxy)-3-phenyl-propionic acid methyl ester

Toluene (160 mL) was added to (R)-3-phenyllactic acid, methyl ester (20g) and p-nitrobenzenesulfonyl chloride (25.8 g) to give a clear yellowsolution which was cooled to 0° C. Triethylamine (16.4 mL) was addedover 15 min, the mixture was stirred at 3° C. for 2 h and then overnightat room temperature. Water (120 mL) was added and the reaction mixturestirred at RT for 1 h. The layers were separated and the organic layerwas washed with water (120 mL). Toluene (20 mL) was added to theresulting organic layer and the solution was heated to remove solvent bydistillation under vacuum (60 mbar) to leave 140 mL solvent in thevessel. Isohexane (120 mL) was added at 40° C. and the mixture wasstirred at this temperature overnight. The mixture was then cooled to25° C. over 115 min and was then filtered. The filter cake was washedwith toluene (20 mL) and isohexane (20 mL), then dried under vacuum at40° C. to give (R)-2-(4-nitro-benzenesulfonyloxy)-3-phenyl-propionicacid methyl ester as a cream solid (31.6 g).

¹H NMR δ_((CDCl3)) 3.0-3.08 (1H, dd), 3.2-3.26 (1H, dd), 3.78 (3H, s),5.0-5.04 (1H, dd), 7.02-7.06 (2H, m), 7.12-7.2 (3H, m), 7.73-7.78 (2H,d), 8.13-8.18 (2H, d).

INTERMEDIATE 25

This illustrates the preparation of(R)-3-(4-fluoro-phenyl)-2-(4-nitro-benzenesulfonyloxy)-propionic acidmethyl ester

(R)-3-(4-Fluorophenyl)-2-hydroxypropionic acid methyl ester (20 g) and4-nitrobenzenesulfonyl chloride (22.8 g) were dissolved inmethylisobutyl ketone (240 mL). The solution was cooled to 0-5° C. andtriethylamine (10.74 g) was added dropwise over 15 min. The reactionmixture was stirred at 0-5° C. for 2 hours. Water (80 mL) was added andthe mixture heated to 35-40° C. to obtain a clear biphasic solution. Theaqueous layer was removed and the organic phase washed successively withdilute hydrochloric acid (1M, 80 mL) and then water at 35-40° C. Theorganic phase was concentrated by distillation under reduced pressure at35-40° C. to a final volume of about 120 mL. To the resulting slurry ofthe product was added isohexane (120 mL) and the mixture cooled to 0-5°C. for 2 h. The solid was filtered, washed with isohexane (60 mL) andthen dried in a vacuum oven at 40° C. under reduced pressure to yieldthe title compound as a yellow solid (32.64 g).

¹H NMR δ_((CDCl3)) 3.02-3.10 (1H, dd), 3.18-3.24 (1H, dd), 3.73 (3H, s),6.85-6.91 (2H, m), 7.03-7.07 (2H, m), 7.86 (2H, d), 8.25 (2H, d).

INTERMEDIATE 26

This illustrates the preparation of(S)-2-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-phenyl-propionicacid methyl ester

Water (90 mL) was added to4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidinedi-benzenesulfonate salt (30 g) to give a suspension. The suspension wasstirred at room temperature for 2 min to give a clear solution.Tert-butyl methyl ether (150 mL) was then charged in one portion and thevessel contents were warmed to 30° C. A solution of 10M Sodium Hydroxide(13.9 g) in water (90 mL) was added over 2 min and the solution wasstirred at 30° C. for 10 min then the layers were separated. The organiclayer was evaporated to dryness, acetonitrile (100 mL) was added and theevaporation was continued until the volume equalled 80 mL. Acetonitrile(70 mL) was then added and to this solution was added potassiumcarbonate (7.8 g) followed by a solution of(R)-2-(4-nitro-benzenesulfonyloxy)-3-phenyl-propionic acid methyl ester(16.3 g) in acetonitrile (30 mL). The resulting suspension was heated to60° C. and held at this temperature overnight. The mixture was cooled to20° C. then tert-butyl methyl ether (150 mL) was added. The suspensionwas filtered and the vessel and cake were washed with tert-butyl methylether (30 mL). The filtrate was washed with 5% brine (90 mL). The layerswere separated and the organic layer was washed with ammoniumacetate/acetic acid solution (72 mL; 15 g Ammonium acetate in 1 L 0.5 Maqueous acetic acid) at 25° C. and then warmed to 40° C. whereuponhydrochloric acid (1M, 90 mL) was added. The layers were separated, theorganic layer was re-extracted with hydrochloric acid (1M, 30 mL) andthen the aqueous phases were combined. Tert-butyl methyl ether (150 mL)and 2M Sodium Hydroxide (90 mL) were added and the mixture stirred at40° C. for 10 min before the phases were separated. The organic phasewas reduced in vacuo to a low volume then ethanol (120 mL) was added anddistillation was continued for a short time till some of the ethanol hadbeen removed. Ethanol (5 mL) was added to the residue (volume 90 mL) andthe solution seeded with(S)-2-{4-[4-(3,4-Dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-phenyl-propionicacid methyl ester (50 mg) and the mixture was cooled to 5° C. over 3 h.A colourless solid was collected by filtration, the cake was washed withethanol (15 mL) and the solid dried under vacuum at 35° C. overnight togive the title compound (16.3 g).

INTERMEDIATE 27

This illustrates the preparation of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid methyl ester

4-[4-(3,4-Dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidinedi-benzenesulfonate salt (40 g) was dissolved in water (120 mL). To thestirred solution was added methyl t-butylether (320 mL), followed by asolution of sodium hydroxide (10M, 22.25 mL) in water (120 mL). Thesolution was heated at 25-30° C. for 20 minutes. The organic layer wasseparated from the aqueous and about 200 mL of the solvent was removedby distillation at atmospheric pressure. To the residue was addedacetonitrile (200 mL) and further solvent removed by distillation to afinal volume of about 240 mL. Karl-Fisher analysis of this solutionindicated 0.35% w/w water was present. To this solution of the free basein acetonitrile was added potassium carbonate (10.40 g) and a solutionof 3-(4-fluorophenyl)-2-(4-nitrobenzenesulfonyloxy)-propionic acidmethyl ester (22.80 g) in acetonitrile (24 mL—prepared by heating theacetonitrile to 35° C.). A small amount of solid residue was washed inwith acetonitrile (16 mL). The reaction mixture was heated at 60-65° C.for 16 h, then cooled to room temperature and methyl t-butylether (200mL) added. After stirring at room temperature for 20 minutes, theprecipitated salts were filtered and washed with methyl t-butylether (40mL). The filtrate was stirred successively with sodium chloride solution(5% w/v in water, 120 mL), ammonium acetate solution (96 mL, 0.2Mammonium acetate in 0.5M aqueous acetic acid solution) and sodiumchloride solution (5% w/v, 120 mL), each for 10 minutes. The organiclayer was separated and solvent distilled off to a final volume of about120 mL. To the residue was added acetonitrile (120 mL) and the volumereduced to about 120 mL (the final distillate temperature was 78-80°C.). The residue was diluted with acetonitrile (120 mL). A sample waswithdrawn and evaporated and weighed to indicate that this solutioncontained about 33 g of the title compound in 240 mL of acetonitrile.

¹H NMR δ_((CDCl3)) 1.18-2.30 (2H, m), 1.4-1.56 (1H, m), 1.74-1.90 (4H,m), 1.90-1.93 (2H, m), 2.13-2.25 (5H, m), 2.3-2.4 (4H, m), 2.6-2.7 (2H,m), 2.8-2.98 (2H, m), 2.98-3.10 (2H, m), 3.35-3.41 (1H, m), 3.6 (3H, s),4.25-4.35 (1H, s), 6.9-6.70 (1H, d), 6.91-6.97 (2H, m), 7.12-7.26 (3H,m).

MS (ES+ve) 537 (M+H)+ INTERMEDIATE 28

This illustrates the preparation of4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}cyclopentane-1,2-diol

a)4-(4-Chloro-2-methylphenoxy)-1-(cyclopent-3-en-1-ylcarbonyl)piperidine

4-(4-Chloro-2-methylphenoxy)piperidine hydrochloride (28.6 g) andtriethylamine (45.5 mL) were stirred in dichloromethane (100 mL) andcyclopent-3-ene-1-carbonyl chloride (14.26 g) in dichloromethane (100mL) was added dropwise. When addition was complete, the reaction mixturewas stirred at room temperature for 2 h. Water (250 mL) was added to thereaction mixture and product was extracted with dichloromethane. Thedichloromethane was washed with brine, dried (MgSO₄), filtered andconcentrated in vacuo. The crude product was filtered through a plug ofsilica eluting with diethyl ether to give the subtitle compound (29.5g).

Retention Time (standard): 2.63

MS (ES+): 320/322 [M+H]⁺

¹H NMR δ_((CDCL3)) 1.76-1.98 (4H, m), 2.21 (3H, s), 2.53-2.64 (2H, m),2.69-2.77 (2H, m), 3.29-3.38 (1H, m), 3.46-3.54 (1H, m), 3.68-3.77 (3H,m), 4.49-4.56 (1H, m), 5.68 (2H, d), 6.75 (1H, d), 7.06-7.15 (2H, m)

b)4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]carbonyl}cyclopentane-1,2-diol

4-(4-Chloro-2-methylphenoxy)-1-(cyclopent-3-en-1-ylcarbonyl)piperidine(29.5 g), N-methylmorpholine-N-oxide (37 g) and potassium osmatedihydrate (0.85 g) were stirred in a mixture of acetone (200 mL) andwater (50 mL) overnight. A saturated solution of sodium metabisulphite(200 mL) was added and the mixture was stirred for 15 min. Product wasextracted with dichloromethane. The dichloromethane was washed withammonium chloride solution then with brine, dried (MgSO₄), filtered andconcentrated in vacuo to give the subtitle compound (32.0 g) as amixture of 2 stereoisomers.

Retention Time (standard) 1.74 and 1.85 min

MS (ES+) 354/356 [M+H]⁺; base peak: 226

c)4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}cyclopentane-1,2-diol

4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]carbonyl}cyclopentane-1,2-diol(32.0 g) was dissolved in tetrahydrofuran (100 mL) and stirred, at roomtemperature, under nitrogen. Borane (1 M solution in THF; 300 mL) wasadded dropwise and then the reaction mixture was heated under reflux for2 h. The reaction mixture was allowed to cool slightly and methanol (60mL) was added carefully. Heating was resumed and continued overnight.The reaction mixture was concentrated in vacuo and the residue waspurified using SCX resin: Non-basic impurities were eluted with methanolthen product was eluted with 0.7 M ammonia in methanol. Solvent wasremoved in vacuo to give the title compound (30 g) as a mixture of 2stereoisomers.

Retention Time (standard) 1.51

MS (ES+) 340/342 [M+H]⁺

INTERMEDIATE 29

This illustrates the preparation of methyl(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoate

4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}cyclopentane-1,2-diol(13.18 g) was dissolved in water (85 ml). Acetic acid (2.22 ml) andsodium periodate (8.38 g) were added. The mixture was then stirred undernitrogen for 30 min. Potassium carbonate (6.97 g) was added and thesolution was diluted with water and extracted into chloroform (210 ml)and then dichloromethane (2×120 ml). The combined extracts were washedwith brine, dried over magnesium sulfate and then poured directly into asolution of methyl 4-fluoro-α-methyl-L-phenylalaninate (8.196 g), sodiumtriacetoxyborohydride (18.91 g) and acetic acid (2.22 ml) indichloromethane (35 ml). The resultant mixture was stirred undernitrogen for 1 h. The solution was poured into saturated sodiumbicarbonate solution (1 l). The mixture was extracted withdichloromethane (3×500 ml). The extracts were dried over magnesiumsulfate and evaporated in vacuo. The crude material was purified bychromatography on neutral alumina (wetted with 5% water, 1 kg) elutingwith 1:1 isohexane:ethyl acetate to give the subtitle compound (15.5 g)as an oil.

MS ESI (+ve) 517/519 (M+H)⁺

Retention Time (fast gradient) 2.03 min.

INTERMEDIATE 30

This illustrates the preparation of methyl(2R)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoate

Prepared following the method of Intermediate 29 using methyl4-fluoro-a-methyl-R-phenylalaninate.

MS ESI (+ve) 517/519 (M+H)⁺

Retention Time (fast gradient) 2.24 min.

EXAMPLE 1

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid

A solution of lithium hydroxide monohydrate (0.162 g) in water was addedto a stirred solution of2-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid methyl ester (0.52 g) in tetrahydrofuran (6 ml) and methanol (2ml). The mixture was stirred at room temperature overnight. Ammoniumacetate (3 g) in water (5 mL) was added followed by ether (10 mL). Themixture was stirred for 1 h then a white solid was collected byfiltration. 100 mg was further purified by RP HPLC (gradient ammoniumacetate:acetonitrile 95:5-5:95) to give the title compound (80 mg).

MS [M−H]⁻ (APCI-) 521/523

Retention time (standard) 1.89

¹H NMR δ_((CD3D)): 1.15-1.39 (2H, m), 1.51-1.66 (1H, m), 1.74-1.88 (4H,m), 1.95-2.08 (2H, m), 2.25 (2H, d), 2.31-2.45 (7H, m), 2.64-2.74 (2H,m), 2.84 (1H, dd), 2.98-3.12 (3H, m), 3.17 (1H, dd), 4.39-4.49 (1H, m),6.90-6.98 (3H, m), 7.23-7.32 (3H, m).

The following compounds were prepared from the corresponding ester usingthe method of Example 1:

MS [M + H]⁺ Example Name (APCI+) ¹H NMR δ_((CD3OD)) 2(2S)-2-[4-[[4-(3,4- 535/537 1.15-1.41 (2H, m), 1.50-1.66 (1H,dichloro-2-methyl- m), 1.72-1.88 (4H, m), 1.95-2.06 phenoxy)-1- (2H, m),2.25 (2H, d), 2.30-2.45 (7H, piperidyl]methyl]-1- m), 2.63-2.75 (2H, m),2.90 (1H, t), piperidyl]-3-(2- 3.02-3.14 (3H, m), 3.25-3.37 (1H,methoxyphenyl)- m), 3.83 (3H, s), 4.38-4.48 (1H, m), propanoic acid 6.80(1H, t), 6.90 (2H, dd), 7.13 (1H, t), 7.22-7.31 (2H, m). 3 (2S)-3-(4-530/532 1.15-1.36 (2H, m), 1.51-1.66 (1H, cyanophenyl)-2-[4- m),1.74-1.88 (4H, m), 1.96-2.07 [[4-(3,4-dichloro-2- (2H, m), 2.25 (2H, d),2.31-2.46 (7H, methyl-phenoxy)-1- m), 2.64-2.74 (2H, m), 2.93-3.22piperidyl]methyl]-1- (5H, m), 4.39-4.49 (1H, m), 6.93 (1H,piperidyl]-propanoic d), 7.29 (1H, dd), 7.47 (2H, d), 7.60 acid (2H, dd)13 (2S)-2-[4-[[4-(3,4- 519/521 1.12 (3H, t), 1.16-1.37 (2H, m), 1.48-dichloro-2-ethyl- 1.63 (1H, m), 1.71-1.86 (4H, m), 1.96- phenoxy)-1-2.05 (2H, m), 2.23 (2H, d), 2.31-2.44 piperidyl]methyl]-1- (4H, m),2.63-2.72 (2H, m), 2.76- piperidyl]-3- 2.90 (3H, m), 2.94-3.03 (1H, m),3.04- phenylpropanoic acid 3.14 (2H, m), 3.18-3.25 (1H, m), 4.39-4.48(1H, m), 6.90 (1H, d), 7.07- 7.13 (1H, m), 7.19 (2H, t), 7.23-7.29 (3H,m) 14 (2S)-2-[4-[[4-(3,4- 537/539 1.11 (3H, t), 1.16-1.35 (2H, m), 1.50-dichloro-2-ethyl- 1.62 (1H, m), 1.71-1.86 (4H, m), 1.96- phenoxy)-1-2.05 (2H, m), 2.23 (2H, d), 2.30-2.43 piperidyl]methyl]-1- (4H, m),2.62-2.71 (2H, m), 2.75- piperidyl]-3-(4- 2.90 (3H, m), 2.95-3.09 (3H,m), 3.11- fluorophenyl)- 3.19 (1H, m), 4.39-4.47 (1H, m), propanoic acid6.87-6.95 (3H, m), 7.22-7.28 (3H, m) 15 (22S)-2-(4-{[4-(3- 494/4961.16-1.39 (2H, m), 1.51-1.67 (1H, chloro-4-cyano-2- (M − H, m),1.74-1.93 (4H, m), 2.00-2.11 methylphenoxy)- ES−) (2H, m), 2.26 (2H, d),2.33 (3H, s), 2.35- piperidin-1- 2.47 (4H, m), 2.64-2.73 (2H, m),yl]methyl}piperidin-1- 2.85 (1H, dd), 2.99-3.16 (3H, m), 3.23yl)-3-phenylpropanoic (1H, dd), 4.57-4.67 (1H, m), 7.07- acid 7.17 (2H,m), 7.19-7.31 (4H, m), 7.62 (1H, d) 16 (2S)-2-(4-{[4-(3- 514/5161.13-1.32 (2H, m), 1.49-1.63 (1H, chloro-4-cyano-2- m), 1.74-1.91 (4H,m), 2.00-2.11 methylphenoxy)- (2H, m), 2.25 (3H, d), 2.33 (3H, s), 2.37-piperidin-1- 2.45 (3H, m), 2.63-2.74 (2H, m), yl]methyl}piperidin-1-2.91-3.08 (4H, m), 3.43 (1H, dd), 3.58 yl)-3-(4-fluorophenyl)- (3H, s),4.56-4.66 (1H, m), 6.96-7.04 propanoic acid (2H, m), 7.09 (1H, d),7.19-7.24 (2H, m), 7.61 (1H, d) 17 (2S)-2-[4-[[4-(2,4- 523/525 1.16-1.39(2H, m), 1.51-1.67 (1H, dichloro-3-methyl- m), 1.74-1.91 (4H, m),1.95-2.06 phenoxy)-1- (2H, m), 2.25 (2H, d), 2.31-2.43 (4H,piperidyl]methyl]-1- m), 2.45 (3H, s), 2.66-2.76 (2H, m),piperidyl]-3-(4- 2.81-2.89 (1H, m), 3.00-3.18 (4H, fluorophenyl)- m),4.42-4.51 (1H, m), 6.94 (3H, t), propanoic acid 7.24-7.30 (3H, m) 18(2S)-2-[4-[[4-(4- 489/491 1.16-1.39 (2H, m), 1.50-1.64 (1H,chloro-2-methyl- m), 1.75-1.87 (4H, m), 1.96-2.07 phenoxy)-1- (2H, m),2.19 (3H, s), 2.25 (2H, d), 2.30- piperidyl]methyl]-1- 2.42 (4H, m),2.64-2.74 (2H, m), piperidyl]-3-(4- 2.86 (1H, dd), 3.00-3.17 (4H, m),4.35- fluorophenyl)- 4.44 (1H, m), 6.86-6.97 (3H, m), propanoic acid7.07-7.12 (2H, m), 7.24-7.30 (2H, m) 19 (2S)-2-[4-[[4-(2,4- 509/5111.16-1.39 (2H, m), 1.51-1.67 (1H, dichloro-phenoxy)-1- m), 1.74-1.91(4H, m), 1.96-2.07 piperidyl]methyl]-1- (2H, m), 2.26 (2H, d), 2.33-2.44(4H, piperidyl]-3-(4- m), 2.66-2.76 (2H, m), 2.87 (1H, d),fluorophenyl)- 3.06 (3H, t), 3.15 (1H, d), 4.44-4.54 propanoic acid (1H,m), 6.94 (2H, t), 7.10 (1H, d), 7.23- 7.31 (3H, m), 7.40 (1H, dd)

EXAMPLE 4

This Example illustrates the preparation of(S)-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid

A mixture of methyl(S)-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoate(123 mg), barium hydroxide (130 mg), tetrahydrofuran (2 ml), water (1ml) and methanol (1 ml) were heated together in the microwave at 190° C.for 2.5 h. The mixture was then acidified with acetic acid (1 ml),concentrated, and purified by reverse-phase hplc (95:5 0.1% aqueousammonium acetate/acetonitrile to 5:95 0.1% aqueous ammoniumacetate/acetonitrile over 10 minutes, symmetry column to give the titlecompound (109 mg).

¹H NMR δ_((CD3OD)) 1.00 (3H, s), 1.18-1.35 (2H, m), 1.48-1.62 (1H, m),1.70-1.81 (4H, m), 1.94-2.04 (2H, m), 2.16-2.45 (6H, m), 2.71 (3H, d),3.03-3.16 (2H, m), 3.23 (1H, d), 4.32-4.43 (1H, m), 6.89 (3H, t), 7.08(1H, d), 7.25 (2H, t), 7.37 (1H, d).

MS (ES+ve) 523/525 (M+H)⁺

The following compounds were prepared from the corresponding ester usingthe method of Example 4:

MS [M + H]⁺ Example Name (APCI+) ¹H NMR δ_((CD3OD)) 5(S)-2-[4-[[4-(4-chloro-2- 503/505 1.00 (3H, s), 1.20-1.36 (2H, m), 1.50-methyl-phenoxy)-1- 1.63 (1H, m), 1.71-1.85 (4H, m), 1.94-piperidyl]methyl]-1- 2.04 (2H, m), 2.17 (3H, s), 2.19-2.25piperidyl]-3-(4- (3H, m), 2.29-2.44 (3H, m), 2.63-2.74fluorophenyl)-2-methyl- (3H, m), 3.03-3.16 (2H, m), 3.22 (1H, propanoicacid d), 4.33-4.42 (1H, m), 6.85-6.92 (3H, m), 7.05-7.10 (2H, m), 7.25(2H, dd) 6 (S)-2-[4-[[4-(3,4- 537/539 1.00 (3H, s), 1.21-1.36 (2H, m),1.49- dichloro-2-methyl- 1.63 (1H, m), 1.71-1.86 (4H, m), 1.95-phenoxy)-1- 2.06 (2H, m), 2.16-2.26 (3H, m), 2.28- piperidyl]methyl]-1-2.44 (3H, m), 2.31 (3H, s), 2.62-2.75 piperidyl]-3-(4- (3H, m),3.02-3.17 (2H, m), 3.22 (1H, fluorophenyl)-2-methyl- d), 4.37-4.46 (1H,m), 6.85-6.93 (3H, propanoic acid m), 7.21-7.29 (3H, m) 12 Isomer 4 of2-[4-[[4-(3,4- 519/521 0.96 (3H, d), 1.15-1.33 (2H, m), 1.44-dichloro-2-methyl- 1.59 (1H, m), 1.66-1.82 (4H, m), 1.89- phenoxy)-1-2.02 (2H, m), 2.08-2.43 (9H, m), 2.56- piperidyl]methyl]-1- 2.72 (4H,m), 3.05 (2H, d), 4.32-4.43 piperidyl]-2-methyl-3- (1H, m), 6.83-6.91(1H, m), 7.02-7.16 phenyl-propanoic acid (3H, m), 7.17-7.27 (3H, m)

EXAMPLE 11

This Example illustrates the preparation of Isomer 3 of2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-2-methyl-3-phenylpropanoicacid.

Methyl2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-2-methyl-3-phenylpropanoate(Isomer 3; 177 mg), 6M hydrochloric acid (20 ml) and isopropyl alcohol(10 ml) were heated together at 98° C. for 22 days. The mixture was thencooled, concentrated and purified by reverse-phase hplc using 95:5 0.1%aqueous ammonium acetate/acetonitrile to 5:95 0.1% aqueous ammoniumacetate/acetonitrile over 10 minutes, symmetry column, to give the titlecompound (38 mg).

MS [M−H]⁻ 519/521 (APCI-)

¹H NMR δ_((CD3OD)): 1.01 (3H, s), 1.24-1.35 (2H, m), 1.50-1.62 (1H, m),1.71-1.87 (4H, m), 1.96-2.05 (2H, m), 2.15-2.26 (4H, m), 2.30 (3H, s),2.32-2.43 (2H, m), 2.61-2.75 (3H, m), 3.01-3.18 (2H, m), 3.25 (1H, d),4.38-4.46 (1H, m), 6.91 (1H, d), 7.08-7.29 (6H, m).

The following compounds were prepared from the corresponding ester usingthe method of Example 11:

MS [M + H]⁺ Example Name (APCI+) ¹H NMR δ_((CD3OD)) 8 Isomer 1 of2-[4-[[4-(3,4- 505/507 1.01 (3H, s), 1.17-1.37 (2H, m), 1.50-dichlorophenoxy)-1- 1.62 (1H, m), 1.70-1.82 (4H, m), 1.94-piperidyl]methyl]-1- 2.06 (2H, m), 2.15-2.47 (6H, m), 2.66-piperidyl]-2-methyl-3- 2.76 (4H, m), 3.05-3.18 (2H, m), 4.34-phenyl-propanoic acid 4.42 (1H, m), 6.88 (1H, dd), 7.07-7.13 (2H, m),7.17 (2H, t), 7.25 (2H, d), 7.37 (1H, d) 9 Isomer 2 of 2-[4-[[4-(3,4-505/507 1.01 (3H, s), 1.19-1.36 (2H, m), 1.50- dichlorophenoxy)-1- 1.63(1H, m), 1.76 (4H, d), 1.95-2.04 piperidyl]methyl]-1- (2H, m), 2.16-2.26(4H, m), 2.31 (2H, t), piperidyl]-2-methyl-3- 2.43 (1H, t), 2.65-2.76(3H, m), 3.13 phenyl-propanoic acid (2H, t), 4.34-4.43 (1H, m),6.87-6.90 (1H, m), 7.08-7.13 (2H, m), 7.17 (2H, t), 7.25 (2H, d), 7.37(1H, d) 10 (±)-2-[4-[[4-(3,4- 519/521 1.01 (3H, s), 1.24-1.35 (2H, m),1.50- dichloro-2-methyl- 1.62 (1H, m), 1.71-1.87 (4H, m), 1.96-phenoxy)-1- 2.05 (2H, m), 2.15-2.26 (4H, m), 2.30 piperidyl]methyl]-1-(3H, s), 2.32-2.43 (2H, m), 2.61-2.75 piperidyl]-2-methyl-3- (3H, m),3.01-3.18 (2H, m), 3.25 (1H, phenyl-propanoic acid d), 4.38-4.46 (1H,m), 6.91 (1H, d), 7.08- 7.29 (6H, m)

EXAMPLE 20

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid sodium salt

(2S)-2-[4-[[4-(3,4-Dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid (1.0 g) was suspended in methanol. Sodium hydroxide (79 mg) inwater (1 ml) was added and the resulting solution was stirred for 1 hand then the solvent was evaporated. The residue was dissolved inethanol (50 ml) at reflux and then allowed to cool. The volume wasreduced to 30 ml by evaporation and the resulting solution was left tocrystallise overnight. Collection of the resultant crystals gave thetitle compound (0.6 g).

Melting point: 227-229° C.

2.48% water by Karl Fisher analysis

¹H NMR δ_((CD3OD)): 1.10-1.26 (2H, m), 1.43-1.53 (1H, m), 1.62-1.75 (4H,m), 1.85-1.95 (2H, m), 2.13 (2H, d), 2.21 (3H, s), 2.18-2.27 (2H, m),2.33 (2H, t), 2.53-2.62 ((2H, m), 2.67-2.75 (1H, m), 2.86-2.95 (1H, m),2.96-3.07 (2H, m), 3.11-3.17 (1H, m), 4.26-4.36 (1H, m), 6.81 (1H, d),7.01 (1H, t), 7.10 (2H, t), 7.13-7.20 (3H, m).

EXAMPLE 21

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid sodium salt

This compound was prepared following the method of Example 20 using(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid and recrystallising by stirring with isopropanol.

Melting point: 230-232° C.

¹H NMR δ_((CD3OD)) 1.13-1.40 (2H, m), 1.53-1.68 (1H, m), 1.75-1.89 (4H,m), 1.96-2.08 (2H, m), 2.25 (2H, d), 2.31-2.50 (7H, m), 2.66-2.75 (2H,m), 2.82 (1H, dd), 2.98-3.15 (3H, m), 3.22 (1H, dd), 4.38-4.49 (1H, m),6.91-7.00 (3H, m), 7.25-7.32 (3H, m).

EXAMPLE 22

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid potassium salt

This compound was prepared following the method of Example 20 using(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid and potassium hydroxide. The initial product from evaporation ofthe solvent was resuspended in methanol and evaporated and thensuspended in diethyl ether and evaporated to give the title compound.

Melting point: 210-214° C.

EXAMPLE 23

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid methanesulfonic acid salt

(2S)-2-[4-[[4-(3,4-Dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid (1.0 g) was suspended in methanol-water (3:1, 30 mL).Methanesulfonic acid (190 mg) was added and the mixture was heated underreflux until solution was obtained. The solution was cooled and thesolvent was evaporated. Recrystallisation from ethanol gave the titlecompound (0.9 g)

Melting point: 225-228° C.

3.09% water by Karl Fisher analysis

¹H NMR δ_((CD3OD)) 1.54-1.71 ((2H, m), 2.00-2.29 (7H, m), 2.35 (3H, s),2.70 (3H, s), 2.98-3.07 (2H, m), 3.10 (2H, d), 3.23 (2H, d), 3.27-3.43(4H, m), 3.53 (1H, d), 3.65 (1H, d), 3.75-3.84 (1H, m), 4.63-4.73 (1H,m), 6.96 (1H, d), 7.20-7.26 (1H, m), 7.26-7.39 (5H, m).

EXAMPLE 24

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-phenylpropanoicacid benzenesulfonic acid salt

This compound was prepared following the method of Example 23 usingbenzenesulfonic acid. The salt crystallised directly on cooling theinitial solution.

Melting point: 160-162° C.

2.4% water by Karl Fisher analysis.

¹H NMR δ_((CD3OD)) 1.55-1.71 (2H, m), 2.00-2.27 (7H, m), 2.34 (3H, s),2.98-3.13 (4H, m), 3.23 (2H, d), 3.26-3.43 (4H, m), 3.52 (1H, d), 3.64(1H, d), 3.79 (1H, t), 4.61-4.71 (1H, m), 6.96 (1H, d), 7.19-7.26 (1H,m), 7.27-7.35 (5H, m), 7.39-7.46 (3H, m), 7.81-7.86 (2H, m).

EXAMPLE 25

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid benzenesulfonic acid salt

This compound was prepared following the method of Example 24.

Melting point: 259-260° C.

EXAMPLE 26

This Example illustrates the preparation of(2S)-2-[4-[[4-(3,4-dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid hydrochloride

(2S)-2-[4-[[4-(3,4-Dichloro-2-methyl-phenoxy)-1-piperidyl]methyl]-1-piperidyl]-3-(4-fluorophenyl)-propanoicacid (0.75 g) was suspended in ether and a solution of HCl in dioxane(4M, 0.37 mL) was added. The mixture was stirred overnight and thenevaporated. The residue was treated with ether and then evaporated andthis procedure was repeated several times until a free-flowing solid wasobtained. This solid was dried under vacuum at 50° C. overnight. Theresultant solid was suspended in methanol with warming and thencollected and dried to give the title compound (0.55 g)

Melting point: 281-283° C.

EXAMPLE 26

This illustrates the preparation of2-Benzyl-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)butanoicacid

This compound was prepared from methyl2-benzyl-2-(4-{[4-(3,4-dichlorophenoxy)piperidin-1-yl]methyl}piperidin-1-yl)butanoatefollowing the method of Example 4 to give the title compound

MS (APCI⁺) 519/521 (M+H⁺)

EXAMPLE 27

This illustrates the preparation of(S)-2-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-phenyl-propionicacid

Tetra-n-butylammonium hydroxide (3.12 g) was dissolved in acetonitrile(5 mL) and added to a suspension of(S)-2-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-phenyl-propionicacid methyl ester (1.0 g) in acetonitrile (9 mL) at room temperature.The mixture was stirred at this temperature for 3 h then methyltert-butyl ether (10 mL) was added, followed by water (4 mL). A solutionof ammonium acetate (0.89 g) in water (5 mL) was added causing theproduct to precipitate from solution. The mixture was stirred for 3 h atroom temperature and then filtered. The filter cake was washed withwater (50 mL) and methyl tert-butyl ether (20 mL). The product was driedunder vacuum at 40° C. to give the title compound (0.88 g).

EXAMPLE 28

This illustrates the preparation of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid (Form I)

To(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid methyl ester (1 g) in acetonitrile (9 mL) solution (Intermediate28) was added a solution of tetra-n-butylammonium hydroxide (3.31 g, 48%w/w in water) in acetonitrile (5 mL) over 10 minutes at 20° C.

The reaction mixture was stirred at 20-22° C. for 2 hours.Methyl-tert-butyl ether (10 mL) was added to the reaction mixturefollowed by a solution of ammonium acetate (0.87 g) in water (5 mL).After 1 h of stirring at room temperature water (5 mL) was added. Theprecipitate formed was stirred overnight at room temperature.

The solid was filtered and washed (slurry wash) with water (2×4 mL) andmethyl tert-butylmethyl ether (6 mL). The solid was dried at 40° C.under reduced pressure overnight to yield the title compound as acolourless solid (0.44 g; melting point 230-237° C., starts degrading at220° C.).

¹H NMR δ_((CD3OD)) 1.25-1.40 (2H, m), 1.5-1.65 (1H, m), 1.70-1.90 (4H,m), 1.92-2.10 (2H, m), 2.20-2.25 (2H, m), 2.35 (3H, s), 2.35-2.42 (4H,m) 2.6-2.75 (2H, m), 2.78-2.90 (1H, m), 2.97-3.20 (4H, m), 4.38-4.50(1H, m), 6.85-7.00 (3H, m), 7.20-7.30 (3H, m) MS (ES+ve) 523 (M+H)⁺.

XRPD of Form I is shown in FIG. 1.

Pos. [°2Th.] d-spacing [Å] Rel. Int. [%] 2.2272 39.63447 50.62 2.691432.79941 35.64 5.3443 16.52252 1.17 7.1482 12.35663 100 8.75 10.097823.57 10.7172 8.24831 6.89 12.6424 6.9962 2.39 13.2608 6.67132 10.3514.0758 6.28685 2.26 14.2953 6.19079 2.23 15.1222 5.85406 1.09 15.99175.53767 5.72 17.8742 4.95848 2.63 18.2983 4.8445 7.36 18.7722 4.7232621.26 19.2498 4.60712 7.52 19.7833 4.48407 4.5 20.1738 4.39815 3.3421.237 4.1803 2.3 22.2454 3.99304 1.4 23.3765 3.80232 2.41 24.35553.65165 5.04 24.6251 3.61229 5.33 25.4107 3.50236 2.98 25.9888 3.425751.53 26.3646 3.37776 1.87 26.8953 3.31231 1.55 31.2745 2.85777 0.7933.0542 2.70785 1.22 34.2844 2.61345 1.18

EXAMPLE 29

This illustrates the preparation of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid (Form II)

To(S)-{4-[4-(3,4-Dichloro-2-methylphenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluorophenyl)-propionicacid methyl ester (5 g) in acetonitrile (40 mL) was added a solution oftetra-n-butylammonium hydroxide (15.10 g, 48% w/w in water) inacetonitrile (25 mL) over 10 minutes between 10-20° C. The reactionmixture was stirred at 20-22° C. for 2 h. To the reaction mixture wasadded a solution of ammonium acetate (4.35 g) in water (50 mL) forming aprecipitate. A small amount of the solid was withdrawn, isolated byfiltration and washed with water three times. The XRPD analysis of thissolid indicated that it was form II. The slurry was then stirredovernight at room temperature. A sample of the slurry was again checkedby XRPD which showed that it was now form I. The solid was filtered andwashed (slurry wash) with water (3×20 mL). The solid was dried in theoven at 40° C. under reduced pressure overnight to yield the titlecompound as a colourless solid (3.60 g).

XRPD for Form II is shown in FIG. 2

Pos. [°2Th.] d-spacing [Å] Rel. Int. [%] 2.2315 39.55948 99.14 2.674933.00216 76.85 5.3589 16.47747 3.63 7.186 12.29168 100 8.6551 10.208311.83 10.0439 8.79962 3.1 11.0966 7.96713 1.2 12.1727 7.26509 4.6813.1501 6.72725 14.53 14.3825 6.15345 3.85 15.1743 5.83409 2.28 17.02365.20427 40.99 17.3697 5.10133 64.11 18.5373 4.78257 8.87 19.1233 4.6373167.78 19.3663 4.57968 30.28 20.0799 4.41851 6.99 21.069 4.21325 10.7922.247 3.99275 7.08 22.8768 3.88424 3.31 24.417 3.64259 28.48 25.18343.53346 18.08 27.5786 3.23177 3.67 33.7683 2.6522 1.92 34.6377 2.587596.2 38.741 2.32245 1.74

EXAMPLE 30

This illustrates the preparation of(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)propanoicacid

A Methyl(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)propanoate

Powdered sieves (20 g, 4 Å) were added to a solution of methyl(2R)-3-(4-fluorophenyl)-2-hydroxypropanoate (32 g) in dichloromethane(200 mL). The mixture was stirred, under nitrogen, at room temperature,for 15 min then cooled to 0° C. Triflic anhydride (29.9 mL) was added,followed, after 10 min, by 2,6-lutidine (41.4 mL), which was added overapproximately 1 h. Stirring was continued for 1 h at 0° C. A solution of4-(3,4-dichloro-2-methylphenoxy)-1-(piperidin-4-ylmethyl)piperidine(57.6 g) in dichloromethane (600 mL) was added at such a rate that theinternal temperature did not exceed 5° C. Triethylamine (49.5 mL) wasadded dropwise and the mixture was stirred at 0° C. for 1 h. Thereaction mixture was filtered through a plug of silica; washing throughwith dichloromethane. The filtrate was reduced in volume by evaporationunder reduced pressure and then washed (×2) with water. The organicfraction was dried (MgSO₄), filtered and concentrated in vacuo to givethe title compound as a brown oil.

B(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)propanoicacid

A solution of lithium hydroxide monohydrate (27.0 g) in water (180 mL)was added dropwise to an ice cooled solution of methyl(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)propanoate(from step A) in methanol (115 mL) and THF (450 mL). The mixture wasstirred at room temperature overnight. A solution of ammonium acetate(165 g) in water (300 mL) was added to the reaction mixture, followed bydiethyl ether (550 mL). The two phase mixture was stirred rapidly for5.5 h then solid was collected. The solid was washed with water (2×300mL) and diethyl ether (3×300 mL) and then dried in a vacuum oven at 40°C. overnight (batch one).

A second batch of solid was collected from the filtrate after standingfor 24 h. This was similarly washed with water and diethyl ether thendried (batch two).

Lithium hydroxide monohydrate (1 eq in water) was added to a mixture ofbatch one in methanol and THF. The free acid was precipitated byaddition of ammonium acetate in water. Once again, two crops of crystalswere obtained at different time points (batches three and four). Batchthree was treated with lithium hydroxide and then ammonium acetate asbefore to produce two further crops (batches five and six).

The lithium salt of batch two was prepared by addition of lithiumhydroxide monohydrate (1 eq in water). This solution was extracted withdichloromethane. A solution of ammonium acetate in water was added tothe dichloromethane layer and a solid precipitated which was collectedby filtration (batch seven).

Batches four, six and seven were combined and dried to give the titlecompound (31.19 g).

¹H NMR δ_((CD3OD+1 drop NaOD)) 1.25 (2H, ddd), 1.50-1.61 (1H, m),1.72-1.84 (4H, m), 1.94-2.02 (2H, m), 2.22 (2H, d), 2.27-2.40 (7H, m),2.61-2.68 (2H, m), 2.82 (1H, dd), 2.99-3.08 (3H, m), 3.13 (1H, dd),4.36-4.43 (1H, m), 6.87-6.95 (3H, m), 7.22-7.27 (3H, m).

MS 521/523 [M−H]⁻ (APCI-)

EXAMPLE 31

This illustrates the preparation of(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-phenylpropanoicacid

A Methyl(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-phenylpropanoate

Powdered sieves (20 g, 4 Å) were added to a solution of methyl(2R)-2-hydroxy-3-phenylpropanoate (32.8 g) in dichloromethane (200 mL).The mixture was stirred, under nitrogen, at room temperature, for 15 minthen cooled to 0° C. Triflic anhydride (33.7 mL) was added, followed,after 10 min, by 2,6-lutidine (46.7 mL), which was added overapproximately 1 h. Stirring was continued for 1 h at 0° C. A solution of4-(3,4-dichloro-2-methylphenoxy)-1-(piperidin-4-ylmethyl)piperidine(65.0 g) in dichloromethane (600 mL) was added at such a rate that theinternal temperature did not exceed 5° C. Triethylamine (55.8 mL) wasadded dropwise and the mixture was stirred at 0° C. for 1 h. Thereaction mixture was filtered through a plug of silica; washing throughwith dichloromethane. The filtrate was reduced in volume by evaporationunder reduced pressure and then washed (×2) with water. The organicfraction was dried (MgSO₄), filtered and concentrated in vacuo to givethe title compound as a brown oil.

B(2S)-2-(4-{[4-(3,4-Dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-phenylpropanoicacid

A solution of lithium hydroxide monohydrate (30.5 g) in water (180 mL)was added dropwise to an ice cooled solution of methyl(2S)-2-(4-{[4-(3,4-dichloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-phenylpropanoate(from step A) in methanol (115 mL) and THF (450 mL). The mixture wasstirred at room temperature overnight. A solution of ammonium acetate(165 g) in water (300 mL) was added to the reaction mixture, followed bytert-butylmethyl ether (300 mL). The two phase mixture was stirredrapidly for 2 h. The solid was collected, washed with water (3×300 mL)and diethyl ether (3×200 mL). The solid was added to diethyl ether andstirred for 1 h then filtered. Fresh diethyl ether was added and thestirring, filtering procedure was repeated. The solid obtained was driedunder vacuum at 50° C. overnight to give the title compound (33 g).

¹H NMR δ_((CD3OD+1 drop NaOD)) 1.16-1.35 (2H, m), 1.50-1.62 (1H, m),1.72-1.84 (4H, m), 1.94-2.03 (2H, m), 2.22 (2H, d), 2.27-2.39 (7H, m),2.59-2.69 (2H, m), 2.85 (1H, dd), 3.01-3.09 (3H, m), 3.16 (1H, dd),4.36-4.44 (1H, m), 6.89 (1H, d), 7.11 (1H, dt), 7.17-7.27 (5H, m).

MS 503/505 [M−H]− (APCI-) EXAMPLE 32

This illustrates the preparation of(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid hydrate (Form A)

Methyl(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoate(34.5 g) and 50% aqueous hydrobromic acid (1.5 l) were heated togetherat 160° C. for 72 h. The hydrobromic acid was then removed in vacuo. Theresulting solid was dissolved in a 3:1 mixture of acetonitrile:water(350 ml) and a solution of lithium hydroxide monohydrate (7 g) in water(50 ml) was added. A solution of ammonium acetate (15.42 g) in water (30ml) was then added, followed by isohexane (150 ml). The mixture was thenstirred vigorously for 1 h. and allowed to stand for 1 h. The solidprecipitate was collected, washed well with diethyl ether and driedovernight in vacuo. The solid was recrystallised from 3:1acetonitrile:water (400 ml) to give the title compound (21 g) as achannel hydrate (Form A).

3.85% water (Karl-Fischer analysis)

MS ES+ (+ve) 503/505 (M+H)⁺

¹H NMR δ_((CD3OD)) 1.32 (3H, s), 1.41-1.68 (2H, m), 1.72-1.84 (3H, m),1.85-2.13 (4H, m), 2.15 (3H, s), 2.24-2.29 (2H, m), 2.31-2.41 (2H, m),2.61-2.76 (2H, m), 2.96-3.09 (3H, m), 3.18 (1H, d), 3.32-3.40 (1H, m),3.59-3.72 (1H, m), 4.30-4.42 (1H, m), 6.85 (1H, d), 6.96 (2H, t),7.03-7.11 (2H, m), 7.23-7.31 (2H, m)

XRPD for Form A is shown in FIG. 3

Pos. [°2Th.] d-spacing [Å] Rel. Int. [%] 5.3042 16.64746 38.18 10.60818.33289 15.1 12.2996 7.19041 21.34 12.9368 6.83768 17.84 13.8637 6.38254100 15.4899 5.71594 21.07 15.9475 5.55295 43.36 16.9292 5.23307 45.2119.6122 4.52282 46.88 20.0506 4.4249 39.58 20.4452 4.34037 43.68 21.11484.20421 37.21 21.4664 4.13615 17.97 22.5577 3.93845 5.89 23.5073 3.781475.72 24.0362 3.69943 31.3 24.7697 3.59152 30.35 25.1369 3.53988 10.0425.8045 3.4498 15.74 26.74 3.33119 9.4 27.8356 3.20251 4.01 29.3993.03566 11.28 29.642 3.01133 11.65 31.3761 2.84874 7.22 32.3322 2.766657.42 33.6764 2.65923 5.23 34.41 2.6042 4.99 35.8167 2.50508 4.12

EXAMPLE 33

This illustrates the preparation of(2R)-2-(4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid

This was prepared following the method of Example 32 using methyl(2R)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoate.

¹H NMR δ_((CD3OD)) 1.31 (3H, s), 1.50 (1H, q), 1.62 (1H, q), 1.73-1.84(2H, m), 1.85-2.12 (5H, m), 2.16 (3H, s), 2.31 (2H, d), 2.35-2.46 (2H,m), 2.66-2.78 (2H, m), 2.95-3.11 (3H, m), 3.18 (1H, d), 3.36 (1H, d),3.60-3.71 (1H, m), 4.33-4.43 (1H, m), 6.86 (1H, d), 6.96 (2H, t),7.03-7.11 (2H, m), 7.26 (2H, t)

MS (ES−ve) 501/503 (M−H)⁺

EXAMPLES 34(2S)-2-(4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid Form B

(2S)-2-(4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid (for example amorphous or crystalline) can initially be partlydissolved in an organic solvent and stirred until Form B is obtained.The process involves a solution mediated transformation in the slurrywithout complete dissolution of the starting material. Thistransformation is thermodynamically driven to yield a more stable formwith a lower solubility under the conditions evaluated.

Form B is typically formed when a slurry of Form A of(2S)-2-(4-{[4-(4-chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid is stirred in ethanol at 25° C. or 60° C. for greater than 1 day.

XRPD for(2S)-2-(4-{[4-(4-Chloro-2-methylphenoxy)piperidin-1-yl]methyl}piperidin-1-yl)-3-(4-fluorophenyl)-2-methylpropanoicacid ethanol solvate Form B is shown in FIG. 4

Pos. [°2Th.] d-spacing [Å] Rel. Int. [%] 7.6772 11.50625 32.02 8.90789.91929 3.67 13.307 6.64824 100 13.7582 6.43123 6.47 15.2087 5.8209632.61 15.4305 5.73779 15.65 16.3607 5.41362 6.19 17.3791 5.09859 18.0118.3842 4.82206 71.89 19.6742 4.5087 87.16 20.0571 4.42348 6.95 20.64394.29904 13.54 21.6962 4.09284 43.29 22.7189 3.91087 19.79 23.06113.85361 8.87 24.3742 3.6489 5.79 26.3108 3.38455 2.6 26.7429 3.330834.82 29.037 3.07268 1.93 29.8487 2.99095 1.32 32.0179 2.79309 2.41

EXAMPLE 35

Histamine H1 receptor binding activity of compounds of the invention wasassessed by competition displacement of 1 nM [3H]-pyrilamine (Amersham,Bucks, Product code TRK 608, specific activity 30 Ci/mmol) to 2 μgmembranes prepared from recombinant CHO-K1 cells expressing the human H1receptor (Euroscreen SA, Brussels, Belgium, product code ES-390-M) inassay buffer (50 mM Tris pH 7.4 containing 2 mM MgCl₂, 250 mM sucroseand 100 mM NaCl) for 1 hour at room temperature.

The following compounds of the invention gave inhibition of[3H]pyrilimine binding:

Example H1 pKi 3 7.5 4 7.1 6 7.5 13 7.0

EXAMPLE 36 Eotaxin-2-Induced Shape Change in Eosinophils in Human BloodIn Vitro

See for example, Differential regulation of eosinophil chemokinesignaling via CCR3 and non-CCR3 pathways. Sabroe I, Hartnell A, JoplingL A, Bel S, Ponath P D, Pease J E, Collins P D, Williams T J. J.Immunol. 1999 Mar. 1; 162(5):2946-55.

Human blood, collected by venous puncture into 9 mL lithium-heparintubes, was incubated with the CCR3 agonist eotaxin-2 in the presence ofvehicle (0.1% (v/v) DMSO) or test compound for 4 min at 37° C. in adeep, 96-square-well plate. The blood was fixed with Optilyse B (100 μL)at room temperature for 10 min and then the red blood cells were lysedwith distilled water (1 mL) for 60 min at room temperature.

The plate was centrifuged at room temperature for 5 min at 300 g. Thepellet was re-suspended in assay buffer (PBS without CaCl₂ and MgCl₂,containing HEPES (10 mM), Glucose (10 mM) and 0.1% (w/v) BSA, pH 7.4))and the samples were analysed using flow cytometry (FC500, BeckmanCoulter). The high autofluorescence of eosinophils allowed them to beidentified as a discrete population from the other blood cell types.Eosinophil shape was monitored as the refractive index of the eosinophilpopulation as determined using the forward scatter signal in flowcytometry.

Eotaxin-2 induced a concentration-dependent change in the forwardscatter of eosinophils and these data were used to construct aconcentration effect curve (E/[A] curve). The rightward displacement ofthe eotaxin-2 E/[A] curve in the presence of a CCR3 antagonist was usedto estimate a pA₂ value in blood using the following equation:

Single pA ₂=−log₁₀ ([B]/(r−1))

where r is the ratio of the concentrations required for half maximaleffects of eotaxin-2 in the absence and presence of antagonist ([A]₅₀for eotaxin-2 in the presence of antagonist divided by [A]₅₀ for controleotaxin-2 curve) and [B] is the molar concentration of antagonist.

The following compounds of the invention gave inhibition ofshape-change:

Example CCR3 pA₂ 1 7.3 2 7.7 3 7.7 4 7.6 5 7.9 6 8.2 12 8.0 13 6.7 146.7 16 7.1 20 7.2 21 7.3 22 7.3 23 7.2 24 7.2 25 7.3 26 7.3

EXAMPLE 37 Determination of Compound Affinity at Human Recombinant CCR3Receptors Assessed by Competition of[³H]-4-(2,4-dichloro-3-methylphenoxy)-1′-[4-(methylsulfonyl)benzoyl]-1,4′-bipiperidinefor CHO-K1 Cell Membranes In Vitro

Membranes, prepared from CHO-K1 cells stably expressing recombinanthuman CCR3, suspended in assay buffer (50 mM Tris-Base, pH 7.4;containing sodium chloride (100 mM) and magnesium chloride (2 mM)) wereincubated in the presence of 2 nM[³H]-4-(2,4-dichloro-3-methylphenoxy)-1′-[4-(methylsulfonyl)benzoyl]-1,4′-bipiperidine,along with vehicle (1% (v/v) DMSO),4-(4-chloro-3-methylphenoxy)-1′-[2-(methylsulfonyl)benzoyl]-1,4′-bipiperidine(to define non-specific binding) or test compound for 2 h at 37° C. inround bottomed 96-well plates. The plates were then filtered onto GF/Bfilter plates, pre-soaked for 1 hour in plate-coating solution (0.3%(w/v) polyethylenimine, 0.2% (w/v) BSA in de-ionised water), using a96-well plate Tomtec cell harvester. Four washes (250 μL) with washbuffer (50 mM Tris-Base, pH 7.4 containing sodium chloride (500 mM) andmagnesium chloride (2 mM)) were performed at 4° C. to remove unboundradioactivity. Plates were dried and MicroScint-O (50 μL) was added toeach well. The plates were sealed (TopSeal A) and filter-boundradioactivity was measured with a scintillation counter (TopCount,Packard BioScience) using a 1 minute counting protocol.

Specific binding was determined from values of the control wells minusthe values for the NSB wells for each assay plate. pIC₅₀ values werecalculated using a four parameter logistic fit (where pIC₅₀ is definedas the negative logarithm of the concentration of compound required for50% reduction in specific[³H]-4-(2,4-dichloro-3-methylphenoxy)-1′-[4-(methylsulfonyl)benzoyl]-1,4′-bipiperidinebinding). Data were presented as mean pKi values (calculated by applyinga Cheng-Prussof correction to pIC₅₀ values) from a minimum of 2 separateexperiments.

The following compounds of the invention gave inhibition of binding:

Example CCR3 pKi 1 9.3 2 9.2 3 9.3 4 9.1 5 9.2 6 9.7 8 7.6 9 8.6 10 8.311 8.8 12 9.7 13 8.9 14 9.3 15 8.2 16 8.9 17 9.3 18 8.4 19 8.3 20 8.7 219.3 22 9.3 23 8.7 24 8.7 25 9.3 26 9.3

1. The compound(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid, or a pharmaceutically acceptable salt thereof.
 2. Apharmaceutically acceptable salt of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid which is a sodium, potassium or (CH₂CH₂OH)₃NH⁺ salt, or ahydrochloride, dihydrochloride, hydrobromide, phosphate, sulfate,acetate, fumarate, maleate, malonate, succinate, tartrate, citrate,oxalate, methanesulfonate, benzenesulfonate or p-toluenesulfonic acidsalt.
 3. The compound(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid.
 4. A polymorph of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid (Form I) having an X-ray powder diffraction pattern containingspecific peaks at: 2.2 (±0.1°), 2.7 (±0.1°), 7.1 (±0.1°), 10.7 (±0.1°),13.3 (±0.1°) and 18.8 (±0.1°) 2θ.
 5. A polymorph of(S)-{4-[4-(3,4-dichloro-2-methyl-phenoxy)-piperidin-1-ylmethyl]-piperidin-1-yl}-3-(4-fluoro-phenyl)-propionicacid (Form II) having an X-ray powder diffraction pattern containingspecific peaks at: 2.2 (±0.1°), 2.67 (±0.1°), 7.2 (±0.1°), 13.2 (±0.1°),17.0 (±0.1°), 17.4 (±0.1°), 19.1 (±0.1°), 19.4 (±0.1°), 21.1 (±0.1°),24.4 (±0.1°) and 25.2 (±0.1°) 2θ.
 6. A pharmaceutical composition whichcomprises a compound of formula (I), or a pharmaceutically acceptablesalt thereof, as claimed in claim 1, or a salt as claimed in claim 2,and a pharmaceutically acceptable adjuvant, diluent or carrier.